Crystallography Open Database

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Searching journal of publication like 'Organic Letters' volume of publication is 6

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1506951 CIFC12 H18 O5P 1 21 18.6269; 6.722; 10.4529
90; 92.173; 90
605.73Bravo, Fernando; McDonald, Frank E.; Neiwert, Wade A.; Hardcastle, Kenneth I.
Alkene substituents for selective activation of endo-regioselective polyepoxide oxacyclizations.
Organic letters, 2004, 6, 4487-4489
1506952 CIFC11 H17 Br O4P 32 2 17.208; 7.208; 42.0575
90; 90; 120
1892.36Bravo, Fernando; McDonald, Frank E.; Neiwert, Wade A.; Hardcastle, Kenneth I.
Alkene substituents for selective activation of endo-regioselective polyepoxide oxacyclizations.
Organic letters, 2004, 6, 4487-4489
1506953 CIFC56 H34 F24 O3 P2P -112.7183; 15.7674; 16.5468
67.448; 67.65; 71.824
2780.2Wu, Hai-Chen; Yu, Jin-Quan; Spencer, Jonathan B.
Stereospecific deoxygenation of phosphine oxides with retention of configuration using triphenylphosphine or triethyl phosphite as an oxygen acceptor.
Organic letters, 2004, 6, 4675-4678
1506954 CIFC48 H28 F12 O2 P2C 1 2/c 128.7227; 8.4943; 17.9976
90; 109.824; 90
4130.8Wu, Hai-Chen; Yu, Jin-Quan; Spencer, Jonathan B.
Stereospecific deoxygenation of phosphine oxides with retention of configuration using triphenylphosphine or triethyl phosphite as an oxygen acceptor.
Organic letters, 2004, 6, 4675-4678
1506955 CIFC56 H34 F24 O P2P -113.3186; 14.8047; 15.3134
85.932; 72.993; 73.854
2773.35Wu, Hai-Chen; Yu, Jin-Quan; Spencer, Jonathan B.
Stereospecific deoxygenation of phosphine oxides with retention of configuration using triphenylphosphine or triethyl phosphite as an oxygen acceptor.
Organic letters, 2004, 6, 4675-4678
1506956 CIFC48 H28 F12 P2C 1 2/c 128.4224; 8.0575; 18.7865
90; 110.05; 90
4041.61Wu, Hai-Chen; Yu, Jin-Quan; Spencer, Jonathan B.
Stereospecific deoxygenation of phosphine oxides with retention of configuration using triphenylphosphine or triethyl phosphite as an oxygen acceptor.
Organic letters, 2004, 6, 4675-4678
1506957 CIFC30 H41 N3 O8C 1 2 124.287; 5.089; 26.519
90; 103.94; 90
3181Ray, Sudipta; Haldar, Debasish; Drew, Michael G. B.; Banerjee, Arindam
A new motif in the formation of peptide nanotubes: the crystallographic signature.
Organic letters, 2004, 6, 4463-4465
1506958 CIFC29 H39 N3 O8C 1 2 124.3; 5.062; 25.97
90; 102.882; 90
3114Ray, Sudipta; Haldar, Debasish; Drew, Michael G. B.; Banerjee, Arindam
A new motif in the formation of peptide nanotubes: the crystallographic signature.
Organic letters, 2004, 6, 4463-4465
1506959 CIFC19 H26 N2 O3 SP 21 21 216.9465; 13.0021; 20.3093
90; 90; 90
1834.32Overman, Larry E.; Velthuisen, Emile J.
Stereocontrolled construction of either stereoisomer of 12-oxatricyclo[6.3.1.0(2,7)]dodecanes using Prins-pinacol reactions.
Organic letters, 2004, 6, 3853-3856
1506960 CIFC13 H21 N3 O SP 21 21 217.9972; 11.8432; 14.5588
90; 90; 90
1378.9Overman, Larry E.; Velthuisen, Emile J.
Stereocontrolled construction of either stereoisomer of 12-oxatricyclo[6.3.1.0(2,7)]dodecanes using Prins-pinacol reactions.
Organic letters, 2004, 6, 3853-3856
1506961 CIFC23 H42 O3 S2 SiP -17.323; 17.75; 19.552
81.888; 88.834; 88.885
2515.1Overman, Larry E.; Velthuisen, Emile J.
Stereocontrolled construction of either stereoisomer of 12-oxatricyclo[6.3.1.0(2,7)]dodecanes using Prins-pinacol reactions.
Organic letters, 2004, 6, 3853-3856
1506962 CIFC11 H18 O3 S2C 1 2 114.0471; 7.9277; 11.5877
90; 102.849; 90
1258.11Overman, Larry E.; Velthuisen, Emile J.
Stereocontrolled construction of either stereoisomer of 12-oxatricyclo[6.3.1.0(2,7)]dodecanes using Prins-pinacol reactions.
Organic letters, 2004, 6, 3853-3856
1506963 CIFC23 H32 N2 O3 S3C 1 2/c 161.439; 10.1168; 31.402
90; 97.819; 90
19337Overman, Larry E.; Velthuisen, Emile J.
Stereocontrolled construction of either stereoisomer of 12-oxatricyclo[6.3.1.0(2,7)]dodecanes using Prins-pinacol reactions.
Organic letters, 2004, 6, 3853-3856
1506964 CIFC20 H25 N O6P 1 21/c 112.1406; 13.1539; 12.965
90; 113.258; 90
1902.2Overman, Larry E.; Velthuisen, Emile J.
Stereocontrolled construction of either stereoisomer of 12-oxatricyclo[6.3.1.0(2,7)]dodecanes using Prins-pinacol reactions.
Organic letters, 2004, 6, 3853-3856
1506965 CIFC24 H23 Cl O4P 1 21/c 19.4195; 21.7175; 10.4372
90; 90.8136; 90
2134.9Babu, Srinivasarao Arulananda; Yasuda, Makoto; Shibata, Ikuya; Baba, Akio
In- or in(I)-employed diastereoselective Reformatsky-type reactions with ketones: 1H NMR investigations on the active species.
Organic letters, 2004, 6, 4475-4478
1506966 CIFC20 H20 Br Cl O4P 1 21/a 111.847; 8.94; 19.015
90; 93.27; 90
2011Babu, Srinivasarao Arulananda; Yasuda, Makoto; Shibata, Ikuya; Baba, Akio
In- or in(I)-employed diastereoselective Reformatsky-type reactions with ketones: 1H NMR investigations on the active species.
Organic letters, 2004, 6, 4475-4478
1506967 CIFC17 H19 N O3 SP 1 21/c 115.306; 11.1614; 9.8395
90; 94.631; 90
1675.5Andreana, Peter R.; Liu, Chang C.; Schreiber, Stuart L.
Stereochemical control of the Passerini reaction.
Organic letters, 2004, 6, 4231-4233
1506968 CIFC17 H18 Br N O4P 21 21 219.4372; 20.8127; 36.61
90; 90; 90
7190.7Andreana, Peter R.; Liu, Chang C.; Schreiber, Stuart L.
Stereochemical control of the Passerini reaction.
Organic letters, 2004, 6, 4231-4233
1506969 CIFC10 H12 F2 N2 O3P 1 21/c 16.1123; 19.495; 9.2417
90; 107.676; 90
1049.2Yang, Yan-Yan; Meng, Wei-Dong; Qing, Feng-Ling
Synthesis of 2',3'-dideoxy-6',6'-difluorocarbocyclic nucleosides.
Organic letters, 2004, 6, 4257-4259
1506970 CIFC17 H24 N O2 P SP 41 21 213.6603; 13.6603; 40.766
90; 90; 90
7607.1Kobayashi, Yuka; Morisawa, Fumi; Saigo, Kazuhiko
A new hydrogen-bonding motif for chiral recognition in the diastereomeric salts of racemic 1-phenylethylamine derivatives with enantiopure O-ethyl phenylphosphonothioic acid.
Organic letters, 2004, 6, 4227-4230

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