Table Of Content

MAGNETIC RESONANCE IN CHEMISTRY Magn. Reson. Chem. 37, 921-923 (1999) Author index to Volume 37 Abe, A. Brennan, C. M. Elsevier, C. J. Abraham, R. J. Bringmann, G. ElSohly, H. N. Achari, B. Brouillette, W. J. Engelhardt, G. Adcock, W. Brouwer, E. B. Enright, G. D. Ahlgrén, M. J. Brunner, E. Ernst, H. Al Badri, A. Brunner, W. Ernst, L. Alam, M. Buchanan, G. W. Ernsting, J. M. Albizati, K. F. Burgess, J. P. Eskuche, G. Alén, R. Burguefio-Tapia, E. Esteban, A. L. Alexiou, A. D. P. Alvarez-Larena, A. Cadoni, E. Farfan, N. Amezcua, C. A. Campos, M. P. A. Faure, R. 87, 328, Amoureux, J. P. 223, S55, Campredon, M. Fehér, M. 346 Ando, I. Canet, D. Férey, G. $100 Ando, S. Carvalho, A. P. Fernandez, C. 223, S55, S69 Araya-Maturana, R. Cassels, B. K. Ferreira, A. 912 Arieli, D. Cervantes-Cuevas, H. Figueras, F. $135 Ariza-Castolo, A. Cesare Marincola, F. Figueroa- Villar, J. D. 239 Arnold, J. R. P. Chattopadhyaya, J. Fisher, J. Asakawa, N. Cheetham, A. K. Flores, A. F. C. Avasia, M. Chen, G. Féldesi, A. Chen, Y. Fontaine, C. B.Nagy, J. Chen, Y.-H. Forgo, P. Bailly, A. Chimichi, S. Frahm, A. W. Balasubramanian, M. Chippendale, A. M. Fraissard, J. Balazs, B. Ciesielski, W. Francke, V. Batoniak, S. Clark, A. M. Franz, A. Bambagiotti-Alberti, M. Clement, B. Frenzel, W. Banerjee, S. Clemente, A. Freude, D. Bao, X. Cmoch, P. Fripiat, J. J. Bar, N.-K. Commenges, G. Fudala, L. D. Barkallah, S. Contreras, R. H. Furuya, H. Basosi, R. Coran, S. A. Bauer, W. Cosstick, R. Gaemers, S. Baumeister, U. Costa Bizzarri, P. Galache, M. P. Becker, G. Costa, S. M. O. Galy, J. P. Beeby, A. Crouch, R. C. Gao, H. Beevers, A. P. G. Cruz, E. R. Garcia, F. Belloc, J. Gavin, J. Belton, P. S. Daloze, D. Gawinecki, R. Beltrame, P. Dalvit, C. Gédéon, A. Beltran, H. de Haan, J. W. Gelli, G. Ben Akacha, A. de Kowalewski, D. G. Genoni, F. Berces, A. de Paula e Silva, C. H. T. Geoffroy, M. Berger, S. Dechter, J. J. Gerig, J. T. Bergter, L. Delay, C. Geyer, A. Bernardo, M. Delbaere, S. Ghiviriga, I. Bernatowicz, P. Delevoye, L. Giannellini, V. Bertini, I. Delgado-Castro, T. Gillies, D. G. Besson, G. Della Casa, C. Giraud, A. Biddau, B. Demadrille, R. Giraud, L. Bigan, M. Demeunynck, M. Girreser, U. Blechta, V. Denkova, P. S. Giusti, G. Blinn, J. R. deNys, R. Glaser, S. Blondeau, D. Diez, E. Godoy-Reyes, J. Blumenfeld, A. L. Dimitrov, V. S. Goldfarb, D. Bochu, C. Dokalik, A. Gorrichon, J.-P. Bodart, P. R. Dombi, G. Grabuleda, X. Bodurka, J. Dommisse, R. Grechishkin, V. S. Bohlen, J.-M. Dostal,J . 195, Grima, P. Bohlmann, W. Dovidauskas, S. Groger, S. Bokotey, S. Driega, A. B. Grossmann, G. Bonacorso, H. G. D’ Souza, V. T. Gudat, D. Bonardet, J.-L. Duddeck, H. 371, 751, Giinther, G. Bosdacek, V. Dumazy, Y. Giinther, H. $142 Bottari, P. Q. Dziembowska, T. Gutsze, A. $147 Bottle, S. E. Bourque, K. Ebener, M. Habermehl, G. 371 Braekman, J. C. Eisenhauer, R. Hadden, C. E. 1, 325, 385, 517, 529, 721 Braga, R. M. Eldewik, A. Hagele, G. 389 Braz-Filho, R. Elgamal, M. H. A. Haire, D. L. 251, 767 Brecht, V. Eloranta, J. M. 774 Han, X. W. 140 © 1999 John Wiley & Sons, Ltd. MAGNETIC RESONANCE IN CHEMISTRY, VOL. 37, 921-923 (1999) MAGNETIC RESONANCE IN CHEMISTRY Hanna, A. G. 754 Koivisto, J. 359, 743 Michel, D. $93, $126 Hanoun, J. P. 87 Kolehmainen, E. 163, 359, 407, 437, 743 Mikenda, W. 895 Harbison, G. 299 Korde, S. S. 594 Mikros, E. 498 Harris, K. D. H. 15 Korecz, L. 484 Mildner, T. $38 Harris, R. K. 15, 232, 573, 709 Kovacs, J. 754 Miltsov, S. A. 743 Hartmann, S. 69 Kowalewski, J. 799 Minch, M. J. 788 Haubold, W. 545 Kowalewski, V. J. 31, 227 Mitaku, S. 498 Hayashi, S. 843 Kraft, H. 667 Mitra, A. 687 Hayes, R. G. 583 Kraus, J. 53 Mohammed Hossein, A. A. 693 Heckmann, G. 667 Krishnamurthy, V. V. 517 Mondal, N. B. 152 Heikkinen, S. 821 Kriiger, K. 43 Montaiia, A. 507 Heise, H. 573 Kuczkowiak, U. 827 Monti, G. A. 709 Helm, L. 701 Kiihlmeyer, C. 538 Morales-Rios, M. S. 243 Hempel, G. 376 Kumaki, Y. 413 Morel, S. 87 Hermecz, I. 346 Kumar, N. 157 Morsy, N. A. M. 754 Hernandez, L. R. 430 Kumar, P. 799 Morton, J. R. 353 Hewlins, M. J. E. 65, 445 Kunz, R. W. 91 Moustrou, C. 328 Heydenreich, M. 333 Kupka, T. 421 Mucci, A. 182 Hikichi, K. 413 Kurosu, H. 479 Muccio, D. D. 82 Hilgeroth, A. 376 Kvicalova, M. 427 Mudogo, V. 98 Hill, G. C. 788 Kye, Y.-S. 299 Munch, V. $100 Hohmann, J. 365 Murali, N. 512, 762 Hook, J. M. S63 Laatikainen, R. 119 Murugan, R. 133 H6pfl, H. 682 Lai, A. 600 Nahrstedt, A. 827 Horvath, Gy. 751 Laihia, K. 163, 359, 437, 743 Hosur, R.V. 891 Laister, R. C. 401 Narender, T. 751 Howe, R. F. S63 Lanzi, M. 182 Nascimento, C. 239 Howes, B. D. 538 Lao, W. 157 Ni Dhubhghaill, O. M. 701 Hoyer, F. 371 Lappalainen, K. 163 Nicholson, J. K. 269 Hrvoic, I. 251, 767 Latositiska, J. N. 878, 881 Niecke, E. 43 Hua, W. 149 Laupretre, F. 864 Nieto, P. M. 127 Hubner, G. $23 Leal, K. Z. 676 Nikaido, T. 152, 837 Huchel, U. 145 Lebrun, B. 60 Nikiforov, V. 743 Hudlicky, T. 653 Lee, Y. C. 82 Nikolaou, S. 322 Hufford, C. D. 856 Lemos, T. L. G. 908 Nogaj, B. 878 Hui, Y. Z. 140 Lentz, P. $55 Nordon, A. 15 Humpa, O. 195 Lewandowski, M. 871 Hunger, M. S75 Lewin, A. H. 903 O’Neil Johnson, M. 393 Hurtado-Guzman, C. 312 Lhomme, J. 73 O’Neil Parker, Jr, W. 433 Hwang, L.-P. S84 Li, C. 140 Oepen, S. $142 Li, X.-C. 856 Olechnowicz, R. $147 Iarossi, D. 182 Libot, F. 498 Ortiz, F. S. 31 Ibrom, K. 441 Liedtke, N. 867 Osmiatowski, B. 437 Inoue, Y. 303 Lindon, J. C. 269 Issmaili, S. 591 Linker, T. 53 Paasivirta, J. 359 Lippert, B. 564 Pan, J. 149 Jaime, C. 885 Lisowski, J. 287 Paralta, J. E. 167 Janzen, E. G. 251, 767, 805 Liu, M. 269 Parella, T. 7, 631 Jia, Z. 152, 837 Liu, X. M. 140 Passmore, J. 353 Jobic, H. $79 Lodowski, P. 421 Pasterna, G. 421 Johansson, M. 799 Logan, T. M. 512, 762 Patel, A. B. 279 Jolivet, C. 512, 762 Loiseau, T. $100 Patel, P.K. 891 Jones, B. C. N. M. 814 Lii, M. 149 Pauli, G. F. 827 Joseph-Nathan, P. 243, 430 Liinsmann, D. 167 Perikylad, M. 743 Josey, J. A. 748 Luyten, H. 25 Peralta, J. E. 31 Joshi, B. S. 295 Lycka, A. 133 Permi, P. 821 Jouaiti, A. 735 Perumal, S. 65, 133, 445 Jullian, C. 312 Ma, Y. 269 Pessoa, O. D. L. 908 Magusin, P. C. M. M. $108 Peters, W. 867 Kalchhauser, H. 895 Malkavaara, P. 407 Pfeifer, H. $154 Kalck, P. 127 Maltseva, T. 203 Phadke, R. S. 279 Kaluzny, B. 325 Manttari, P. 163 Piekarska-Bartoszewicz, B. 189 K4nai, K. 346 269 Pilawa, B. 871 Karavan, V. S. 743 195, 781 Piniella, J. F. 885 Karger, J. $38, S79 Marival-Hodebar, L. 579 Pique, V. 87, 591 Katarzyriski, R. 173 Martin, G. E. 1, 325, 385, 517, 529, 721 Podanyi, B. 346 Kato, L. 447 Martinek, T. 365 Pogni, R. 538 Katoch, R. 594 Martins, M. A. P. 852 Poleschner, H. 333 Kauppinen, R. 359, 437, 743 Masierak, W. $147 Pomares, M. 885 Keller, W. 545 Mathias, L. 676 Poppe, L. 382, 748 Kilpeliitien, I. 821 McCallum, C. M. 788 Popp, A. $93 Kjelleberg, S. 157 McCormick, A. V. $27 Potrzebowski, M. 173 Klaui, W. 867 McGeorge, G. 232 Potts, B. C. M. 393 Klik, R. $135 McLaurin, G. E. 353 Povolotskii, M. I. 551 Klimkiewicz, J. 189 Medeiros, W. L. B. 676 Pregosin, P. S. 91, 246 Koch, M. 498 Meizer, E. 493 Preston, K. F. 353 Kohler, F. H. 573 Merbach, A. E. 701 Prosser James, J. 393 Koike, K. 152, 837 Micallef, A. S. 730 Pruski, M. S69 © 1999 John Wiley & Sons, Ltd. MAGNETIC RESONANCE IN CHEMISTRY, VOL. 37, 921-923 (1999) MAGNETIC RESONANCE IN CHEMISTRY Pulkkinen, J. T. Schweng, G. 895 Toma, H. E. Seidl, P. 317 Tordeux, M. Quadrifoglio, F. Seliger, J. 878, 881 Toth, E. Selvaraj, S. 133, 445 Toth, G. 53, 371, 751, Radeglia, R. Senn, H. 672 Tousek, J. Raetz, C. R. H. Shapiro, G. 7 Trivedi, G. Rajendra Kumar, N. Sharaf, M. H. M. , 529 Trujillo-Ferrara, J. Rama Krishna, N. Shimizu, R. 479 Tschoerner, M. Ramakrishna, J. Shultes, M. 799 Tuppurainen, K. Ramesh, K. P. Silks III, L. A. 672 Turano, P. Rankin, S. E. Simon, A. 53 Rao, P. S. Singh, K. L. 295 Udasi, R. A. Read, R. Singh, N. K. S63 Uriarte, E. Rebien, F. Siqueira, G. M. 852 Reichert, D. Sirol, S. 127 van Oers, E. M. Reid, D. A. Skaltsounis, A. 498 van Santen, R. A. Reinsberg, S. A. Sklendar, V. 195, 781 Vanelle, P. Ribeiro, A. A. Slavik, J. 195, 781 Vasas, A. Rivetti, F. Sliwa-Niesci6r, J. $150 Vatanen, V. Robins, R. H. Smirnoy, A. I. 36 Vaughan, D. E. W. Robinson, V. J. Smith, W. B. 103, 107, 110 Vepsalainen, J. J. Rockenbauer, A. Séderman, P. 586 Vermeersch, G. Rodrigues-Filho, E. SoSsnicki, J. 605 Vieira, I. J.C. Roduner, E. Soukupova, L. 427 Vijayabaskar, V. Roland, J. Spano, G. $135 Virgili, A. Rombeck, I. Springuel-Huet, M. SI Vuolle, M. Rosato, A. Spychala, J. 881 Rosch, P. Srivastava, S. 279 Wakselman, C. Roumestand, C. Stebbings, W. L. 613 Wang, G. Roy, R. Stefaniak, L. 493 Wawer, I. Rozhenko, A. B. Stegmann, H. B. 805 Webb, G. Rozwadowski, Z. Steinberg, P. 157 Weigel, S. $100 Riickert, M. Steuernagel, S. 573 Weitkamp, J. S75 Rudolf, T. Stevens, J. 613 Weychert, M. 189 Stocking, E. M. 672 Wichert-Tur, Z. 605 Saeb, W. Strohmaier, K. G. $43 Widmalm, G. 586 Sahu, N. P. Stucky, G. D. $100 Wieckowski, A. B. 871, S150 Saikia, A. Subba Rao, N. 751 Winkler, U. $38 Sakurai, M. Sun, G. 903 Witch, E. M. 814 Salgado-Escobar, I. Sun, Y. 602 Wojtowicz, W. $150 Salmon, M. Suryanarayana, I. 214 Wood, D. J. 353 Salo, H. Sutcliffe, L. H. 36, 730 Wrackmeyer, B. 246, 418, 545 Salzmann, M. Szab6-Planka, T. 484 Wu, X. 36 Sanchez-Ferrando, F. Szeja, W. 421 Santillan, R. Yu, B. 140 Sato, D. Tackie, A. N. 1, 529 Yu, H. 140 Schaber, F.-M. Takenoiri, M. 303 Schenetti, L. Tamminen, J. 163 Zablocki, J. 382 Schenk, U. Taulelle, F. $100 Zakrzewski, A. 437 Schiff Jr, P. L. Taurian, O. E. 31 Zanatta, N. 852 Schilf, W. Teijeira, M. 598 Zantour, H. 916 Schmidt, R. R. Temeriusz, A. 189 Zhang, K. 788 Schoeller, W. W. Teral, Y. 159 Zhou, Z. 620 Schram, J. Teran, C. 598 Zhuo, J.-C. 259 Schripsema, J. Thomann, H. S43 Schuler, P. Tiers, G. V. D. 609, 613 Schuring, D. Tillequin, F. 498 © 1999 John Wiley & Sons, Ltd. MAGNETIC RESONANCE IN CHEMISTRY, VOL. 37, 921-923 (1999) MAGNETIC RESONANCE IN CHEMISTRY Magn. Reson. Chem. 37, 925-927 (1999) Subject index to Volume 37 ab initio calculations 31, 43, 53, 103, 107, 167, bicyclo[3.2.1 Joct-6-en-3-one derivatives 507 dealumination 303, 421, 479, 493, 551, 583, 735, 743, 758, biguanides 662 deoxyribonucleosides 774, 781, 895 bile acids 163 desorption, of NO ACCORD-HMBC 517 binding 269, 279 DFT caculations acetylacetonate complexes 538 biopolymers 203, 564, 891 DFT-NBO calculation acidity, in zeolites S118 biradical 353 deuteron NMR acridines 73, 591 bis-indole alkaloids 676 diamines, 1,3- acridinones 86, 239, 243 bismuth vanadate 223 diarylidenecyclohexanone acronycine derivatives 493 black liquor 407 diastereomers acrylic esters 579 bond population 881 dibenzothiophenes, chlorinated activation parameters 15 borate complex 867 Diels Alder reaction acyclic alcohols, °C chemical shift 214 bovine serum albumin $147 diffusion acyclic alkanes, '*C chemical shift 214 bridging methoxy group $135 —, of benzene acyclovir prodrugs 687 Brgnsted acidity, in zeolites S118 —, of hydrogen in zeolites additivity rule 852 brucine 325 —, of xenon Adina cordifolia 751 bulk drug impurities 393 diglucoside adsorption techniques $142 butanone oxim 433 dihydropyridine, 4-aryl-1,4- adsorption 433, $23, $126 dilution shifts —, of NO $93 C-13 NMR, MAS $38, $108, $135, $142 dinucleosides, 3’-S-PO, linked —., of Xe, review SI caffeoyl quinic acid 827 diorganylseleno salts aggregation 493 cage dimer 376 diosgenins Al-27 NMR, REDOR S118 calix[4]arene 788 dioxaphosphinopyridines — solid state S55, S63, S69 carbamates 885 dipeptide, cyclic alcohols, '"O NMR 852 carbazoles 243 diphenylamines aldonitrones 767 carbohydrates 189, 421, 586 1,5-diphenylipentane-2,4-dione alkaloids 1, 7, 60, 98, 140, 195, 325, 493, 517, carbonucleosides 598 dipolar coupling 676, 751, 781 cardenolides 754 dipolar interaction alkyl halides 609 catalysis $38 disaccharides ALPO S69 —, weakly acidic 433 —, cyclic AIPO,-20 $43 —, basic $75 disproportionation aluminophosphate 3, S69 catalytic transformation 433 diterpenes ametantrone Cd-113 NMR, solid state S63 DNA dodecamers amidinium salts chemical exchange 637 DNA duplex amino acid, fluorinated chemical reactions $38 DNA structures, multi-stranded a-aminoanthraquinone chemical shift anisotropy 223 DNMR aminopyridines chemical shift correlations 333 dodecylphosphocholine micelles 3-aminotropanes chirality 805 double labeling aminoxyls cholanoic acid 163 double quantum filtered NMR ammonia, chemisorbed chromane derivatives 77 drugs 393, amycin B circular dichroism 53 dynamics 15, 173, 317, 346, 365, 564, 586, Ancistrocladus likoko clerodane 430 637, 693, S108, $126 angiotensin III Co-59 NMR 573 dynamics, of DNA duplex 203 anion radicals coal 871 Anthocephalus cadamba cobaltocenium salts 573 E/Z isomerism 69, 82 9,10-anthraquinone derivatives colbaltate complex 867 electric field effect, intramolecular 227 anthracene triones complexes 91 electron delocalization 167 anticancer agent condensation $27 electron density 878, 881 antitumor drug configuration 77, 287, 371, 653, 885 ellagic acid derivatives 856 artifacts —, absolute 53 enaminones 259 aryl complexes, PdX —, of chiral spiro atom 219 enantiomers 53, 269, 287, 885 assignments, NMR 60, 140, 152, 239, 295, conformational analysis 53, 110, 119, 145, ENDOR 805 312, 328, 430, 507, 594, 598, 676, 856, 860, 279, 317, 346, 365, 371, 401, 430, 479, 564, environmental chemistry 743 908, 916 586, 620, 754, 788, 814, 827, 885, 903 enzymes 647 aza sugars 447 continuous flow $14 EPR linewidth $150 azephenalene, perhydro- contrast agent, in MRI 701 EPR 36, 251, 353, 484, 538, 583, 730, 735, azobenzene dyestuffs coordination 484, 701, S63 767, 774, 805, 871, S23, S43, $93, S150 azoloazines copper(II) complexes, EPR 484, 538 ESR, see EPR correlation time 788 ethers, 'O NMR 852 B-10 NMR coumarin, 4-methyl-7-ethoxy- $142 etoposide 53, 788 B-11 NMR coupling constants, see J-coupling exchange $108 B-11{B -11} decoupling CP dynamics, 'H,'°F 709 excitation sculpting 7 ball mill CP/MAS, see solid state NMR excitation 517 basicity, of zeolites cross polarization, J-based 631 EXSY spectroscopy, 2D 15, 637, $108 Beckmann rearrangement cross-conjugation 243 benzene loaded zeolites crown ether analogs 401 F-19 MAS 15, $142 benzene radical cation cryptolepinone 1 F-19 NMR 167, 333, 647, 709 benzenoid aromatics cyclization $27 F-19 RFDR $100 benzofuroxan cyclodextrins 48 F-19 shielding 31, 167 benzohydroxamic acids, silylated cyclohexyl fluorides 167 faujasite-type zeolites S84 benzophenanthridine alkaloids cytosine, 4-N -, derivatives 881 Fe(II) incorporation $43 BET measurements field gradients, see pulsed field gradients bicyclo[2.2.1}heptene derivative DANTE 48, 451 fluorinated groups 579 © 1999 John Wiley & Sons, Ltd. MAGNETIC RESONANCE IN CHEMISTRY, VOL. 37, 925-927 (1999) 926 MAGNETIC RESONANCE IN CHEMISTRY fluorobenzenes 107 isotope shift 243, 274, 609, 667 N-15 NMR 1, 25, 69, 133, 195, 219, 232, 325 fluorocyclohexane 15 385, 427, 433, 493, 602, 662, 895 fluoropolymer 709 J cross polarization 631 Na*-NO complex $93 free radicals 767 J-coupling, #3C,3C 333, 427, 382 NaA zeolite $93 frequency selective filtering 451 418 NaCeY $23 FUCOUP 239 167, 333 NaPdY $23 48, 227, 312, 413, 517, 579, naphthopyran, 3H- 159 gadolinium(III) complexes 701 naphthoquinone dimers 908 gallophosphate $100 195 naphthyl methyl sulfides 445 gases, NMR of 25 333 naphthylisoquinoline alkaloids 98 Gd(II) complexes 701 110, 145, 359, 653, 814, 821 NaPtY $23 Ge-73 NMR 418 385, 748 natural products 287, 365, 371, 430, 493, 512, GIAO calculations 103, 107, 551, 895 545 602, 620, 676, 751, 754, 762, 837, 856, GIAO-CHF calculations 493, 758 916 860, 908 GIAO-DFT calculations 31, 167, 421, 479, 743 333 NaX-type zeolites $126 D-glucitol 447 333 neoadifolin 751 glucopyranosides 189 413, 418 neutron scattering $79 glucose derivatives 421 J-multiplication 821 nitric oxide, adsorption—desorption behaviour glycilglycine 484 $93 glycoside bond 145 ketonitrones 767 nitro groups 843 guanine derivatives 687 B-keto sulfones 437 nitroaniline 843 guest compounds S75 nitrogen dioxide 583 lactones, N-acylhomoserine 157 nitrones 251, 767 H-1 NMR, MAS $126 lanthanide complexes 287 nitroxides 805 H-2 NMR $84 laser heating $38 NMR probe, superconducting 512, 762 Hammett constant Opara+ 91 laser-polarised xenon $14 NMR-NQR double resonance 878, 881 hederagenin 287 LC-NMR 7, 393 NO, adsorption-desorption behaviour heterocycles 65, 73, 77, 86, 127, 133, 149, Lewis acid center $93 NOE, 'H,' 159, 195, 239, 243, 328, 376, 393, 493, 498, Lewis acidity, in zeolites $118 NOESY, 'H of adsorbed molecules 591, 598, 600, 602, 653, 682, 687, 687, 743, Li-aryl 91 norbornadiene, 7-fluoro- 758, 867, 878, 895, 912 lignans 860 norbornane, 7-fluoro- heterocycles, chlorinated 743 lignin 407 7-norborneny] fluorides heteroleptic complexes 867 line broadening 843 N-oxidation hexahydroindazoles 65 lineshape analysis 223, 637 NQR hexamethylbenzene $142 lineshape, EPR 871 nucleic acids 203, 891 hexamethylenetetramine 287 linear prediction 637 nucleoside analogues 598 high pressure cell 25 linewidth, in EPR spectra $150 high pressure NMR 25 Linum usitatissimum 860 O-17 NMR 25, 31, 219, 259, 852, 421, 667, hippodamine 60 Lipari-Szabo order parameter 586 701 history of NMR $154 Lipia sisoides Cham. 908 offretite $55 hopping rates $108 lipids 620 olefins, adsorbed $126 HPLC-NMR 98 liquid crystals 479 oligonucleotides 564 HSQC, selective 48 long-range coupling, heteronuclear 48 oligosaccharides 451 human serum albumin 269 —, interglycosidic 48 organylseleno olefins 333 hydration 788 LSX zeolite $135 y-oxoruthenium acetate cluster 322 hydrazine derivatives 916 LTA zeolites S63 oxovanadium(IV) complexes, EPR 538 hydrazine 65 oxyfluorination $100 hydrazinolysis 149 macrocycles 287, 365 hydrocarbons, polychlorinated 359 magnetometry 251, 767 P-31 hyperfine coupling 735 hydrochlorides 60 maleamic acid 682 P-31 NMR 407, 545, 551, 620, 667, 867, 912, hydrogen diffusion, in zeolites $79 maleimides 682 916, $100 hydrogenation reaction 25 MAS, see solid state NMR P-31 shielding tensor 43 y-hydrogens, effect on '°C chemical shift 214 menthone imine 110 P-31 solid state NMR 43 hydrolysis $27 mesoporous solids S1 palladium(II)-aryl complexes 91 hydrotalcite $135 metabolites 98 [2.2]paracyclophenes 441 hydrothermal treatment $55 metal-to-ligand bonding 91 paramagnetic centers 871 hyperfine coupling 538 methanol-to-gasolin conversion $38 paramagnetic complexes 287 hyperfine tensor, '7O 583 micro cell 359 Pb-207 NMR, solid state $63 micro NVR 721 n-pentane hopping $108 ibuprofen 269, 721 microporous solids Sl peptides 303, 413 IGLO calculations 43 Mimisops elengi 152 phelasin A, B 837 imaging 701, $14, S154 mimusic acid 152 phenanthroline 73 imidazole derivatives 878 mitoxantrone 774 phenyl lithium 91 iminophosphines 43 mixed ligand complexes 867 phosphaalkenes 551, 667, 735 in situ NMR $38 molecular clefts 163 phosphaalkynes 667 INADEQUATE 427 molecular modeling 103, 107, 110, 119, 127, phosphate linkage 620 inclusion compounds 15 401, 493, 788, 837, 885, phosphonylated hydrazones 916 indium 867 molecular sieves 433, $43, S69 B-phosphorus nitroxides 767 indole alkaloids 751 monoterpene derivative 127 phthalazin-1-one derivative 149 indoles 243 MQMAS $55, $69 polarization transfer 382 inhibitor AG2034 393 MRI 701, S14, S154 polyamines 903 internal rotation 317 MTG process $38 poly-2,2'-bithiophene 182 ion pairs 600 multidimensional NMR, review 451 polyboranes 545 IRMA simulations 279 multiple quantum NMR $55, S69 poly-L-alanine 303 isomenthone imine 110 multiple solvent suppression 7 polychlorinated hydrocarbons 359 isoquinoline alkaloids 195 myrthine 60 polymerisation $27 isoquinoline, octahydro- 653 myrtenol hydroformylation 127 polymers 182, 709 isotope effect, see isotope shift N-14 , dipolar interaction 843 polysulfide radical anions $150 © 1999 John Wiley & Sons, Ltd. MAGNETIC RESONANCE IN CHEMISTRY, VOL. 37, 925-927 (1999) MAGNETIC RESONANCE IN CHEMISTRY porosity SI selective experiments 631 succinamic acids porous materials 433, SI-S154 selective filtering 451 succinimids precoccinelline 60 selectivity 451 sucrose pregnenolone selenocystine 672 sulfones prodrugs selenomethionine 173 superconducting NMR probe progesterone self-association 609 supercritical CO, prolyl-endopeptidase inhibitor sensitivity , 162 surface methoxy groups proteins shielding anisotropy 788 surface methyl groups protonation shifts shielding constants 895 protonation sites shielding term, o,,,,4 91 T,, see relaxation pulsed field gradients 1, 7, 631, 647, 721, S79, shift correlation, Yop Ty $100 T,, see relaxation $154 —,N,'H 385, 529, 821 tautomerism 232, 259, 274, 493, 758 pyrazolines 133 Si-29 NMR 427, 667, S27 tecomaquinone 908 pyridine 600 —, REDOR S118 tectol 908 pyridine, 2-amino-3,5-dichloro- 693 —, solid state $55, S63 tensor orientation 223 pyridoazaphosphinines 912 signal enhancement 382, 748 tensor, chemical shift pyrimidothiazine 393 signal-to-noise ratio 512, 762 terminal methoxy group pyrrolidine nitroxide, phosphorylated 251 silane, dimethyldiethoxy $27 tetrakis(trimethylstannyl)germanium silica gel S75 tetralin derivatives quadrupolar effects 573 silica $142 tetramethylsilane solvent quadrupolar interaction 223, 287, 843 silicalite $135 thermal decomposition QUASAR programme 223 silicalite-1 433 topology quasi-elastic neutron scattering $79 silicone $27 torsional angle dynamics 4-quinolinone 243 single crystal EPR study 353 torsional frequency single crystal, NMR of 287 torsional oscillations radical anions $150 SMIGD 385, 529 tricyclic hydrocarbons, polychlorinated radicals, diastereomeric 805 Sn-119 NMR 418 trimethylsilyl derivatives reassignment 322, 441 sodalite $43 trioxacyclooctane, | ,3,6- REDOR $69, S118 sol-gel $27 trioxocane redox reactions $23 solid state NMR 15, 43, 173, 189, 223, 232, triple quantum MAS NMR reference data 82, 86, 157, 159, 163, 328, 445, 287, 303, 376, 479, 573, 709, 843, S38, S55, triterpene 447, 591, 594, 598, 600, 602, 605, 682, 687, $63, S79, $100, $108, S118, $142 triterpenes, pentacyclic 688, 912, 916 solvent effects 827 Tréger’s base regiochemistry, of polymers solvent suppression E regioisomers spin delocalization 735 ubiquitin 821 reinvestigation spin echo NMR, 2D 303 ultramarine blue $150 relaxation 173, 564, 586, 600, 709, 788, S147 spin-lattice relaxation, see relaxation undecanehexaol 371 =. 4 701 spin polarization transfer $14 —, deuteron 203, S84 spin probe, water-soluble 36 V-51 NMR 223 —, NQR spin lattice 693 spin probes 730 variable temperature CP NMR 15 —, rotating frame 15 spin-spin coupling, see J-coupling variable temperature NMR_ 189, 317, 401, 545, —, spin lattice, see relaxation spin trapping 767, 805 637, 709, S38, S108, S150 retinoids 82 spin-hamiltonian engineering $154 variable temperature NQR 693 reviews, on selectivity in multidimensional spiro[4,5]decane 219 NMR 451 stephalic acid 430 water exchange 701 —, on '°Xe NMR S1 stereochemistry 401, 507, 653, 748, 751, 754, water-—protein sojutions $147 —, on laser-polarized 'Xe $14 805, 860, 885 ribonucleosides 814 steric interactions 805 xanthenesione, tetrahydro- 77 ring inversion 15 steroid alkaloids 140 Xe-129 NMR S14 rotational barrier 189 steroids 594 Xe-NMR, review Sl ruthenium clusters 322 —, chemical shifts 103 xenon adsorption Sl stoichiometry 891 X-ray 77, 376, 885, S100 S-33 NMR 437 stop-flow mode 393 salicylaldehyde, 5-nitro 274 structure refinement $100 a-yohimbine 7 salicylaldehydes, 5-X 227 structure 365, 427, 605, 827, 837, 867 saponins 140, 837 strychnine 325, 517, 721 zeolites $23, S38, S55, S63, S75, S79, S84, scalar coupling, see J-coupling submicro NMR 385, 529, 721 $93, $108, $126, $135, $154 Schiff bases 259, 274 substituent effects 852 ZK-S zeolite $108 Se-77 NMR 173, 333, 672 —., of flourine 441, 579 ZSM-5 $38 selective cross poilarisation 382 —, on **S NMR 437 selective excitation 451 —., on chemical shifts 219 © 1999 John Wiley & Sons, Ltd. MAGNETIC RESONANCE IN CHEMISTRY, VOL. 37, 925-927 (1999)