Crystallography Open Database

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Searching journal of publication like 'Organic Letters' volume of publication is 7

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1506495 CIFC48 H100 B40 Si5P c 21 b12.7957; 18.2036; 33.0523
90; 90; 90		7698.8Núñez, Rosario; González, Arántzazu; Viñas, Clara; Teixidor, Francesc; Sillanpää, Reijo; Kivekäs, Raikko
Approaches to the preparation of carborane-containing carbosilane compounds.
Organic letters, 2005, 7, 231-233
1506496 CIFC26 H16 N4 O12P c a 2112.3501; 18.786; 10.827
90; 90; 90		2512Katz, Jeffrey L.; Feldman, Michael B.; Conry, Rebecca R.
Synthesis of functionalized oxacalix[4]arenes.
Organic letters, 2005, 7, 91-94
1506497 CIFC28 H18 N6 O14P 1 n 117.22; 8.4231; 21.729
90; 110.017; 90		2961.3Katz, Jeffrey L.; Feldman, Michael B.; Conry, Rebecca R.
Synthesis of functionalized oxacalix[4]arenes.
Organic letters, 2005, 7, 91-94
1506498 CIFC23 H20 N2 O8P -18.245; 9.07; 15.501
93.34; 91.41; 110.26		1084.4Lu, Chong-Dao; Liu, Hui; Chen, Zhi-Yong; Hu, Wen-Hao; Mi, Ai-Qiao
Three-component reaction of aryl diazoacetates, alcohols, and aldehydes (or imines): evidence of alcoholic oxonium ylide intermediates.
Organic letters, 2005, 7, 83-86
1506499 CIFC30 H28 N2 O7P -19.058; 10.3496; 14.987
74.357; 78.955; 86.161		1327.7Lu, Chong-Dao; Liu, Hui; Chen, Zhi-Yong; Hu, Wen-Hao; Mi, Ai-Qiao
Three-component reaction of aryl diazoacetates, alcohols, and aldehydes (or imines): evidence of alcoholic oxonium ylide intermediates.
Organic letters, 2005, 7, 83-86
1506500 CIFC17 H17 Br O3P 21 21 2112.425; 21.493; 5.9427
90; 90; 90		1587Itoh, Kennosuke; Hasegawa, Masayuki; Tanaka, Junji; Kanemasa, Shuji
Enantioselective enol lactone synthesis under double catalytic conditions.
Organic letters, 2005, 7, 979-981
1506501 CIFC38 H40 N3 O6P -111.852; 15.102; 19.607
74.327; 86.668; 73.37		3237Oguri, Hiroki; Schreiber, Stuart L.
Skeletal diversity via a folding pathway: synthesis of indole alkaloid-like skeletons.
Organic letters, 2005, 7, 47-50
1506502 CIFC43 H47 N7 O10 SP 1 21/n 115.165; 11.97; 22.819
90; 92.248; 90		4139Oguri, Hiroki; Schreiber, Stuart L.
Skeletal diversity via a folding pathway: synthesis of indole alkaloid-like skeletons.
Organic letters, 2005, 7, 47-50
1506503 CIFC21 H20 F6 OP 21 21 28.1817; 18.7309; 6.28
90; 90; 90		962.41Resendiz, Marino J. E.; Garcia-Garibay, Miguel A
Hammett analysis of photodecarbonylation in crystalline 1,3-diarylacetones.
Organic letters, 2005, 7, 371-374
1506504 CIFC30 H31 N O5 SP 1 21 110.905; 9.0569; 13.2693
90; 92.194; 90		1309.59Fernández, Marta; Alonso, Ricardo
Tandem radical addition and cyclization of epsilon-substituted delta-yne ketimines.
Organic letters, 2005, 7, 11-14
1506505 CIFC21 H28 Cl N3 O6P 21 21 216.8995; 16.674; 21.421
90; 90; 90		2464.3Liu, Xiaofeng; Li, Hongming; Deng, Li
Highly enantioselective amination of alpha-substituted alpha-cyanoacetates with chiral catalysts accessible from both quinine and quinidine.
Organic letters, 2005, 7, 167-169
1506506 CIFC14 H4 F4 S4P -16.738; 9.491; 10.247
63.862; 79.987; 76.57		570.27Cho, Don M.; Parkin, Sean R.; Watson, Mark D.
Partial fluorination overcomes herringbone crystal packing in small polycyclic aromatics.
Organic letters, 2005, 7, 1067-1068
1506507 CIFC26 H28 F4 S2P -19.137; 9.74; 13.595
89.465; 73.679; 79.933		1142.23Cho, Don M.; Parkin, Sean R.; Watson, Mark D.
Partial fluorination overcomes herringbone crystal packing in small polycyclic aromatics.
Organic letters, 2005, 7, 1067-1068
1506508 CIFC14 H8 S2P 1 21/n 113.229; 5.055; 16.776
90; 108.127; 90		1066.18Cho, Don M.; Parkin, Sean R.; Watson, Mark D.
Partial fluorination overcomes herringbone crystal packing in small polycyclic aromatics.
Organic letters, 2005, 7, 1067-1068
1506509 CIFC18 H8 F4P 1 21/n 110.989; 6.7478; 16.2987
90; 95.001; 90		1203.97Cho, Don M.; Parkin, Sean R.; Watson, Mark D.
Partial fluorination overcomes herringbone crystal packing in small polycyclic aromatics.
Organic letters, 2005, 7, 1067-1068
1506510 CIFC13 H18 O3P 1 21/c 111.3466; 10.2778; 11.6638
90; 118.642; 90		1193.76Reeder, Matthew D.; Srikanth, G. S. C.; Jones, Spencer B.; Castle, Steven L.
Synthesis of the core structure of acutumine.
Organic letters, 2005, 7, 1089-1092
1506511 CIFC28 H36 Cl2 Cu N2 O4P 1 21 18.7438; 7.6589; 21.3498
90; 90.022; 90		1429.75Lyle, Michael P. A.; Draper, Neil D.; Wilson, Peter D.
Enantioselective Friedel-Crafts alkylation reactions catalyzed by a chiral nonracemic C2-symmetric 2,2'-bipyridyl copper(II) complex.
Organic letters, 2005, 7, 901-904
1506512 CIFC10 H13 N O SP 21 21 215.9008; 9.6079; 17.7589
90; 90; 90		1006.83Fernández, Inmaculada; Valdivia, Victoria; Gori, Beatrice; Alcudia, Felipe; Alvarez, Eleuterio; Khiar, Noureddine
The isopropylsulfinyl group: a useful chiral controller for the asymmetric aziridination of sulfinylimines and the organocatalytic allylation of hydrazones.
Organic letters, 2005, 7, 1307-1310
1506513 CIFC13 H16 Fe O SP 21 21 215.9295; 12.3312; 16.883
90; 90; 90		1234.4Fernández, Inmaculada; Valdivia, Victoria; Gori, Beatrice; Alcudia, Felipe; Alvarez, Eleuterio; Khiar, Noureddine
The isopropylsulfinyl group: a useful chiral controller for the asymmetric aziridination of sulfinylimines and the organocatalytic allylation of hydrazones.
Organic letters, 2005, 7, 1307-1310
1506514 CIFC20 H18P b c a10.7905; 7.675; 17.5436
90; 90; 90		1452.9Lunazzi, Lodovico; Mazzanti, Andrea; Minzoni, Mirko; Anderson, J. Edgar
Structure, conformation, and dynamic processes of the stereolabile atropisomers of hindered terphenyl hydrocarbons.
Organic letters, 2005, 7, 1291-1294
1506515 CIFC26 H30P 1 21/c 18.206; 19.137; 7.029
90; 108.955; 90		1044Lunazzi, Lodovico; Mazzanti, Andrea; Minzoni, Mirko; Anderson, J. Edgar
Structure, conformation, and dynamic processes of the stereolabile atropisomers of hindered terphenyl hydrocarbons.
Organic letters, 2005, 7, 1291-1294
1506516 CIFC14 H22 O2C 1 2/c 119.569; 9.6463; 15.091
90; 116.71; 90		2544.7Heim, Ralf; Wiedemann, Stefan; Williams, Craig M.; Bernhardt, Paul V.
Expedient construction of the vibsanin E core without the use of protecting groups.
Organic letters, 2005, 7, 1327-1329
1506517 CIFC16 H16 N2 O7P -18.3731; 14.2379; 15.576
115.671; 93.9504; 99.789		1627.87Ma, Cheng; Yang, Yewei
Thiazolium-mediated multicomponent reactions: a facile synthesis of 3-aminofuran derivatives.
Organic letters, 2005, 7, 1343-1345
1506518 CIFC20 H16 N4P n a 218.3581; 23.522; 7.8293
90; 90; 90		1539.2Davis, Riju; Tamaoki, Nobuyuki
Novel photochromic spiroheterocyclic molecules via oxidation of 1,8-diaminonaphthalene.
Organic letters, 2005, 7, 1461-1464
1506519 CIFC20 H15 N3 OP 1 21/c 111.993; 16.027; 7.917
90; 97.52; 90		1508.7Davis, Riju; Tamaoki, Nobuyuki
Novel photochromic spiroheterocyclic molecules via oxidation of 1,8-diaminonaphthalene.
Organic letters, 2005, 7, 1461-1464
1506520 CIFC20 H16 N4P 1 21/n 113.904; 4.0318; 14.426
90; 112.209; 90		748.7Davis, Riju; Tamaoki, Nobuyuki
Novel photochromic spiroheterocyclic molecules via oxidation of 1,8-diaminonaphthalene.
Organic letters, 2005, 7, 1461-1464
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

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