Crystallography Open Database

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1506521 CIFC20 H15 N3 OP b c a22.607; 5.3689; 24.359
90; 90; 90
2956.6Davis, Riju; Tamaoki, Nobuyuki
Novel photochromic spiroheterocyclic molecules via oxidation of 1,8-diaminonaphthalene.
Organic letters, 2005, 7, 1461-1464
1506522 CIFC20 H13 N3P 21 21 214.9575; 15.1933; 18.374
90; 90; 90
1383.9Davis, Riju; Tamaoki, Nobuyuki
Novel photochromic spiroheterocyclic molecules via oxidation of 1,8-diaminonaphthalene.
Organic letters, 2005, 7, 1461-1464
1506523 CIFC10 H8 N2 OP 1 21/n 17.4462; 7.8786; 13.6251
90; 91.258; 90
799.13Davis, Riju; Tamaoki, Nobuyuki
Novel photochromic spiroheterocyclic molecules via oxidation of 1,8-diaminonaphthalene.
Organic letters, 2005, 7, 1461-1464
1506524 CIFC20 H15 N3 OP c a 2115.686; 12.04; 7.8796
90; 90; 90
1488.1Davis, Riju; Tamaoki, Nobuyuki
Novel photochromic spiroheterocyclic molecules via oxidation of 1,8-diaminonaphthalene.
Organic letters, 2005, 7, 1461-1464
1506525 CIFC38 H52 N4 O4P -17.8283; 10.626; 11.105
89.465; 75.808; 72.908
854.04Sessler, Jonathan L.; Aguilar, Apolonio; Sanchez-Garcia, David; Seidel, Daniel; Köhler, Thomas; Arp, Forrest; Lynch, Vincent M.
Facile syntheses of quater-, penta-, and sexipyrroles.
Organic letters, 2005, 7, 1887-1890
1506526 CIFC54 H56 F18 N6 O16P -18.5826; 10.7345; 34.6417
88.214; 83.085; 74.848
3058.18Sessler, Jonathan L.; Aguilar, Apolonio; Sanchez-Garcia, David; Seidel, Daniel; Köhler, Thomas; Arp, Forrest; Lynch, Vincent M.
Facile syntheses of quater-, penta-, and sexipyrroles.
Organic letters, 2005, 7, 1887-1890
1506527 CIFC30 H32 N2 O5P 21 21 2110.4318; 14.7988; 35.7592
90; 90; 90
5520.4Wipf, Peter; Stephenson, Corey R. J.
Three-component synthesis of alpha,beta-cyclopropyl-gamma-amino acids.
Organic letters, 2005, 7, 1137-1140
1506528 CIFC19 H18 Br N O3P 21 21 215.3668; 14.348; 23.0874
90; 90; 90
1777.8Wipf, Peter; Stephenson, Corey R. J.
Three-component synthesis of alpha,beta-cyclopropyl-gamma-amino acids.
Organic letters, 2005, 7, 1137-1140
1506529 CIFC18 H21 N O2P 1 21/c 16.8454; 7.4615; 27.2798
90; 91.069; 90
1393.13Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.
Preparation of 2- and 4-arylmethyl N-substituted and N,N-disubstituted anilines via a "green", multicomponent reaction.
Organic letters, 2005, 7, 1525-1528
1506530 CIFC18 H21 N O2P 1 21/c 19.2593; 16.1551; 10.1261
90; 101.834; 90
1482.52Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.
Preparation of 2- and 4-arylmethyl N-substituted and N,N-disubstituted anilines via a "green", multicomponent reaction.
Organic letters, 2005, 7, 1525-1528
1506531 CIFC27 H25 NP n a 2111.8742; 14.427; 11.6716
90; 90; 90
1999.45Rosamilia, Anthony E.; Scott, Janet L.; Strauss, Christopher R.
Preparation of 2- and 4-arylmethyl N-substituted and N,N-disubstituted anilines via a "green", multicomponent reaction.
Organic letters, 2005, 7, 1525-1528
1506532 CIFC18 H14 I2 N4 O2P -15.1091; 8.604; 11.779
96.15; 99.491; 103.281
491.3Goroff, Nancy S.; Curtis, Sean M.; Webb, Jeffrey A.; Fowler, Frank W.; Lauher, Joseph W.
Designed cocrystals based on the pyridine-iodoalkyne halogen bond.
Organic letters, 2005, 7, 1891-1893
1506533 CIFC18 H14 I2 N4 O2P -15.0225; 13.367; 16.614
111.708; 96.629; 90.382
1027.9Goroff, Nancy S.; Curtis, Sean M.; Webb, Jeffrey A.; Fowler, Frank W.; Lauher, Joseph W.
Designed cocrystals based on the pyridine-iodoalkyne halogen bond.
Organic letters, 2005, 7, 1891-1893
1506534 CIFC18 H14 I2 N4 O2P 1 n 14.5341; 33.343; 14.4556
90; 93.812; 90
2180.6Goroff, Nancy S.; Curtis, Sean M.; Webb, Jeffrey A.; Fowler, Frank W.; Lauher, Joseph W.
Designed cocrystals based on the pyridine-iodoalkyne halogen bond.
Organic letters, 2005, 7, 1891-1893
1506535 CIFC18 H14 I2 N4 O2P 1 21/m 14.517; 26.92; 8.586
90; 93.546; 90
1042Goroff, Nancy S.; Curtis, Sean M.; Webb, Jeffrey A.; Fowler, Frank W.; Lauher, Joseph W.
Designed cocrystals based on the pyridine-iodoalkyne halogen bond.
Organic letters, 2005, 7, 1891-1893
1506536 CIFC20 H14 I2 N4 O2P -15.2844; 8.4501; 12.202
77.709; 78.835; 83.769
521Goroff, Nancy S.; Curtis, Sean M.; Webb, Jeffrey A.; Fowler, Frank W.; Lauher, Joseph W.
Designed cocrystals based on the pyridine-iodoalkyne halogen bond.
Organic letters, 2005, 7, 1891-1893
1506537 CIFC20 H14 I2 N4 O2P -14.9734; 9.899; 11.033
96.605; 95.183; 99.824
528.3Goroff, Nancy S.; Curtis, Sean M.; Webb, Jeffrey A.; Fowler, Frank W.; Lauher, Joseph W.
Designed cocrystals based on the pyridine-iodoalkyne halogen bond.
Organic letters, 2005, 7, 1891-1893
1506538 CIFC14 H20 O5 S2P 1 21/c 18.304; 8.875; 20.562
90; 91.997; 90
1514.46Ward, Dale E.; Jheengut, Vishal; Akinnusi, Olukayode T.
Enantioselective direct intermolecular aldol reactions with enantiotopic group selectivity and dynamic kinetic resolution.
Organic letters, 2005, 7, 1181-1184
1506539 CIFC14 H26 O6 S2C 1 2 120.556; 5.32; 15.025
90; 95.915; 90
1634.35Ward, Dale E.; Jheengut, Vishal; Akinnusi, Olukayode T.
Enantioselective direct intermolecular aldol reactions with enantiotopic group selectivity and dynamic kinetic resolution.
Organic letters, 2005, 7, 1181-1184
1506540 CIFC20 H16 O6P 1 21/c 18.0389; 14.888; 14.573
90; 100.433; 90
1715.3Nair, Vijay; Pillai, Abhilash N.; Menon, Rajeev S.; Suresh, Eringathodi
Pyridine-catalyzed addition of diaryl-1,2-diones to dimethyl butynedioate leading to the formation of 1,2-diaroyl dimethyl maleates via an unprecedented rearrangement.
Organic letters, 2005, 7, 1189-1191
1506541 CIFC20 H32 O3P 21 21 216.854; 14.08; 20.093
90; 90; 90
1939.1Jeffery, David W.; Perkins, Michael V.; White, Jonathan M.
Synthesis of the putative structure of tridachiahydropyrone.
Organic letters, 2005, 7, 1581-1584
1506542 CIFC20 H26 O3 SP -19.079; 10.386; 11.448
64.851; 77.443; 72.753
928Souto, José A; López, Carlos Silva; Faza, Olalla Nieto; Alvarez, Rosana; de Lera, Angel R.
2-Alkylidenesulfol-3-enes by (regio- and) stereoselective cheletropic addition of SO2 to (di)vinylallenes.
Organic letters, 2005, 7, 1565-1568
1506543 CIFC28 H30 N O P SiP -19.7494; 12.3191; 12.4391
101.789; 111.839; 107.544
1234.86Ballweg, David M.; Miller, Rebecca C.; Gray, Danielle L.; Scheidt, Karl A.
Stereoselective synthesis of alpha-silylamines by the direct addition of silyl anions to activated imines.
Organic letters, 2005, 7, 1403-1406
1506544 CIFC19 H27 N O S SiP 21 21 216.4269; 16.553; 18.276
90; 90; 90
1944.3Ballweg, David M.; Miller, Rebecca C.; Gray, Danielle L.; Scheidt, Karl A.
Stereoselective synthesis of alpha-silylamines by the direct addition of silyl anions to activated imines.
Organic letters, 2005, 7, 1403-1406
1506545 CIFC17 H33 N O2 S SiP 21 21 216.5692; 15.207; 20.303
90; 90; 90
2028.2Ballweg, David M.; Miller, Rebecca C.; Gray, Danielle L.; Scheidt, Karl A.
Stereoselective synthesis of alpha-silylamines by the direct addition of silyl anions to activated imines.
Organic letters, 2005, 7, 1403-1406
1506546 CIFC66 H71 N9 O13P -110.446; 15.755; 19.741
101.976; 91.797; 98.325
3138Bag, Bamaprasad; Bharadwaj, Parimal K.
Attachment of electron-withdrawing 2,4-dinitrobenzene groups to a cryptand-based receptor for Cu(II)/H+ specific exciplex and monomer emissions.
Organic letters, 2005, 7, 1573-1576
1506547 CIFC69 H67 N7 O7P 1 21/n 112.495; 33.601; 14.107
90; 110.001; 90
5565.53Bag, Bamaprasad; Bharadwaj, Parimal K.
Attachment of electron-withdrawing 2,4-dinitrobenzene groups to a cryptand-based receptor for Cu(II)/H+ specific exciplex and monomer emissions.
Organic letters, 2005, 7, 1573-1576
1506548 CIFC64 H66 Cl N11 O15P -113.143; 13.52; 18.853
85.665; 71.885; 76.671
3098.2Bag, Bamaprasad; Bharadwaj, Parimal K.
Attachment of electron-withdrawing 2,4-dinitrobenzene groups to a cryptand-based receptor for Cu(II)/H+ specific exciplex and monomer emissions.
Organic letters, 2005, 7, 1573-1576
1506549 CIFC75 H80 Cl2 N10 O16P 1 21/c 120.937; 13.542; 24.926
90; 92.507; 90
7060Bag, Bamaprasad; Bharadwaj, Parimal K.
Attachment of electron-withdrawing 2,4-dinitrobenzene groups to a cryptand-based receptor for Cu(II)/H+ specific exciplex and monomer emissions.
Organic letters, 2005, 7, 1573-1576
1506550 CIFC9 H14 O4P b c a9.9387; 11.7542; 15.485
90; 90; 90
1809Aspinall, Helen C.; Greeves, Nicholas; Valla, Carine
Samarium diiodide-catalyzed diastereoselective pinacol couplings.
Organic letters, 2005, 7, 1919-1922
1506551 CIFC29 H36 F3 N2 O3.5C 1 2/c 115.9393; 29.73; 12.2145
90; 92.481; 90
5782.7Nair, Vijay; Sreekumar, V.; Bindu, S.; Suresh, Eringathodi
Two unprecedented multicomponent reactions involving N-heterocyclic carbenes, activated acetylenes, and aldehydes.
Organic letters, 2005, 7, 2297-2300
1506552 CIFC30 H38 F N2 O9P 1 21 19.2322; 17.385; 9.8198
90; 101.64; 90
1543.7Nair, Vijay; Sreekumar, V.; Bindu, S.; Suresh, Eringathodi
Two unprecedented multicomponent reactions involving N-heterocyclic carbenes, activated acetylenes, and aldehydes.
Organic letters, 2005, 7, 2297-2300
1506553 CIFC78 H81 B N2 O2 P2 RuP 1 21 111.791; 17.038; 17.969
90; 74.07; 90
3471.3Guo, Rongwei; Chen, Xuanhua; Elpelt, Christian; Song, Datong; Morris, Robert H.
Applications of ruthenium hydride borohydride complexes containing phosphinite and diamine ligands to asymmetric catalytic reactions.
Organic letters, 2005, 7, 1757-1759
1506554 CIFC81.6 H89.4 B N2 O2 P2 RuP 21 21 2118.059; 18.096; 21.949
90; 90; 90
7173Guo, Rongwei; Chen, Xuanhua; Elpelt, Christian; Song, Datong; Morris, Robert H.
Applications of ruthenium hydride borohydride complexes containing phosphinite and diamine ligands to asymmetric catalytic reactions.
Organic letters, 2005, 7, 1757-1759
1506555 CIFC20 H18 Br Cl OP n a 2127.093; 6.392; 10.547
90; 90; 90
1826.5Sniady, Adam; Wheeler, Kraig A.; Dembinski, Roman
5-Endo-dig electrophilic cyclization of 1,4-disubstituted but-3-yn-1-ones: regiocontrolled synthesis of 2,5-disubstituted 3-bromo- and 3-iodofurans.
Organic letters, 2005, 7, 1769-1772
1506556 CIFC15 H11 Cl O3P 1 21/n 17.8832; 17.578; 9.3048
90; 93.894; 90
1286.4Calter, Michael A.; Tretyak, Olexandr A.; Flaschenriem, Christine
Formation of disubstituted beta-lactones using bifunctional catalysis.
Organic letters, 2005, 7, 1809-1812
1506557 CIFC24 H33 N O5P 1 21 16.9632; 9.5308; 15.805
90; 91.416; 90
1048.6Wu, Huifang; Thatcher, Linn N.; Bernard, Denzil; Parrish, Damon A.; Deschamps, Jeffrey R.; Rice, Kenner C.; MacKerell, Jr, Alexander D; Coop, Andrew
Position of coordination of the lithium ion determines the regioselectivity of demethylations of 3,4-dimethoxymorphinans with L-selectride.
Organic letters, 2005, 7, 2531-2534
1506558 CIFC39 H52 O3P 1 21 114.251; 6.4802; 19.219
90; 97.679; 90
1758.9Kumar, Nilesh; Kiuchi, Masatoshi; Tallarico, John A.; Schreiber, Stuart L.
Small-molecule diversity using a skeletal transformation strategy.
Organic letters, 2005, 7, 2535-2538
1506559 CIFC52 H72 N4 O4P 1 21/c 118.578; 13.143; 21.494
90; 111.874; 90
4870.4Simaan, Samah; Biali, Silvio E.
Preferential axial protonation in a zwitterionic calix[4]arene.
Organic letters, 2005, 7, 1817-1820
1506560 CIFC13 H13 N O6P -18.136; 8.542; 10.627
84.959; 73.671; 69.347
663.2Ding, Hanfeng; Ma, Cheng; Yang, Yewei; Wang, Yanguang
Unexpected reaction of dimethyl acetylenedicarboxylate with in situ generated arylketenes catalyzed by 1-methylimidazole.
Organic letters, 2005, 7, 2125-2127
1506561 CIFC48 H68 N4 O4C 1 2/m 123.64; 16.89; 12.682
90; 116.4; 90
4536Tsue, Hirohito; Ishibashi, Koichi; Takahashi, Hiroki; Tamura, Rui
Exhaustively methylated azacalix[4]arene: preparation, conformation, and crystal structure with exclusively CH/pi-controlled crystal architecture.
Organic letters, 2005, 7, 2165-2168
1506562 CIFC17 H18 N2 O5P 1 21 110.059; 5.9759; 13.3917
90; 108.39; 90
763.89Alvarez de Cienfuegos, Luis; Mota, Antonio J.; Robles, Rafael
Convenient synthesis of nucleoside and isonucleoside analogues.
Organic letters, 2005, 7, 2161-2164
1506563 CIFC13 H18 O3P 1 21 17.872; 7.923; 9.822
90; 98.156; 90
606.4Yasuda, Makoto; Tanaka, Shin-Ya; Baba, Akio
Reductive cross-aldol reaction using bromoaldehyde and an aldehyde mediated by germanium(II): one-pot, large-scale protocol.
Organic letters, 2005, 7, 1845-1848
1506564 CIFC6 H9 N O2P 1 21/c 18.6325; 8.2795; 9.4032
90; 108.713; 90
636.55Hu, Tianshun; Li, Chaozhong
Synthesis of lactams via copper-catalyzed intramolecular vinylation of amides.
Organic letters, 2005, 7, 2035-2038
1506565 CIFC12 H18 N2 O2P b c a7.6969; 9.6905; 16.428
90; 90; 90
1225.3Hu, Tianshun; Li, Chaozhong
Synthesis of lactams via copper-catalyzed intramolecular vinylation of amides.
Organic letters, 2005, 7, 2035-2038
1506566 CIFC69 Cl9 NP 1 21/c 110.1516; 15.4731; 26.0575
90; 100.362; 90
4026.3Pham, David; Cerón Bertran, Jordi; Olmstead, Marilyn M.; Mascal, Mark; Balch, Alan L.
Interaction of fullerenes with the concave surfaces of perchloroazatriquinacene.
Organic letters, 2005, 7, 2805-2808
1506567 CIFC79 Cl9 NP b c a16.844; 19.929; 26.869
90; 90; 90
9019Pham, David; Cerón Bertran, Jordi; Olmstead, Marilyn M.; Mascal, Mark; Balch, Alan L.
Interaction of fullerenes with the concave surfaces of perchloroazatriquinacene.
Organic letters, 2005, 7, 2805-2808
1506568 CIFC6 H11 F2 N O2P 21 21 219.6285; 10.2351; 15.0732
90; 90; 90
1485.4Wang, Ruo-Wen; Qing, Feng-Ling
Highly stereocontrolled synthesis of gem-difluoromethylenated azasugars: D- and L-1,4,6-trideoxy-4,4-difluoronojirimycin.
Organic letters, 2005, 7, 2189-2192
1506569 CIFC18 H23 N O5P 1 21 16.8517; 39.307; 7.0654
90; 115.035; 90
1724.1Morin, Matthew D.; Rychnovsky, Scott D.
Reductive spiroannulation of nitriles with secondary electrophiles.
Organic letters, 2005, 7, 2051-2053
1506570 CIFC18 H23 N O5P 1 21 19.6051; 7.4837; 11.8595
90; 99.663; 90
840.39Morin, Matthew D.; Rychnovsky, Scott D.
Reductive spiroannulation of nitriles with secondary electrophiles.
Organic letters, 2005, 7, 2051-2053

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