Crystallography Open Database
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Searching volume of publication is 6
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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1506930 | CIF | C60 H54 F12 N10 O4 P2 Ru2 | P 1 2/n 1 | 11.413; 12.631; 22.655 90; 95.192; 90 | 3252.5 | Rastegar, Majid F.; Todd, Erin K.; Tang, Hongding; Wang, Zhi Yuan A new class of near-infrared electrochromic oxamide-based dinuclear ruthenium complexes. Organic letters, 2004, 6, 4519-4522 |
1506931 | CIF | C29 H21 N3 O7 | P 1 21/c 1 | 17.2335; 14.9473; 9.4343 90; 97.164; 90 | 2411.2 | Zhang, Yan; Wang, Lei; Zhang, Min; Fun, Hoong-Kun; Xu, Jian-Hua Photoinduced [4 + 4] cycloadditions of o-quinones with oxazoles. Organic letters, 2004, 6, 4893-4895 |
1506932 | CIF | C24 H17 N O3 | P 1 21/c 1 | 10.5543; 12.653; 13.6927 90; 103.879; 90 | 1775.19 | Zhang, Yan; Wang, Lei; Zhang, Min; Fun, Hoong-Kun; Xu, Jian-Hua Photoinduced [4 + 4] cycloadditions of o-quinones with oxazoles. Organic letters, 2004, 6, 4893-4895 |
1506933 | CIF | C25 H22 Cl2 N2 O5 S | P 1 21 1 | 6.3777; 14.081; 14.2429 90; 97.89; 90 | 1267 | Xu, Xin; Kotti, S. R. S. Saibabu; Liu, Junying; Cannon, John F.; Headley, Allan D.; Li, Guigen Ionic liquid media resulted in the first asymmetric aminohalogenation reaction of alkenes. Organic letters, 2004, 6, 4881-4884 |
1506934 | CIF | C36 H26 Cl2 O8 | P 1 21/a 1 | 16.09; 10.544; 17.881 90; 104.605; 90 | 2936 | Saitoh, Terunobu; Yoshida, Suguru; Ichikawa, Junji 1,8-bis(diphenylmethylium)naphthalenediyl dication as an organic oxidant: synthesis of benzidines via self-coupling of N,N-dialkylanilines. Organic letters, 2004, 6, 4563-4565 |
1506935 | CIF | C26 H31 N Si | P b c a | 11.17; 16.42; 24.14 90; 90; 90 | 4428 | Yagi, Kazunari; Shinokubo, Hiroshi; Oshima, Koichiro Synthesis of silyl aziridines and alpha-amino acylsilanes with silyldibromomethyllithium. Organic letters, 2004, 6, 4339-4341 |
1506936 | CIF | C14 H22 N2 O3 | P 1 21/n 1 | 10.6541; 9.4448; 14.5765 90; 109.205; 90 | 1385.1 | Kim, Yi Jin; Lee, Daesung Use of N-N bond stereodynamics in ring-closing metathesis to form medium-sized rings and macrocycles. Organic letters, 2004, 6, 4351-4353 |
1506937 | CIF | C18 H16 N2 O2 | P 1 21/c 1 | 7.423; 14.598; 13.89 90; 92.82; 90 | 1503.3 | Muthyala, Rajeev S.; Subramaniam, Gopal; Todaro, Louis The use of squaric acid as a scaffold for cofacial phenyl rings. Organic letters, 2004, 6, 4663-4665 |
1506938 | CIF | C18 H26 O8 | P 1 21/c 1 | 7.2663; 9.8732; 26.502 90; 95.2; 90 | 1893.5 | Hulin, Bernard; Newton, Linda S.; Cabral, Shawn; Walker, Aaron J.; Bordner, Jon Three-component, stereoselective palladium-catalyzed synthesis of functionalized bicyclopentanoids. Organic letters, 2004, 6, 4343-4345 |
1506939 | CIF | C19 H23 Cl O4 | P 1 21/c 1 | 5.794; 7.595; 40.65 90; 90.91; 90 | 1788.6 | Hulin, Bernard; Newton, Linda S.; Cabral, Shawn; Walker, Aaron J.; Bordner, Jon Three-component, stereoselective palladium-catalyzed synthesis of functionalized bicyclopentanoids. Organic letters, 2004, 6, 4343-4345 |
1506940 | CIF | C20 H24 O5 | P -1 | 8.748; 9.689; 11.773 81.91; 85.5; 66.42 | 905.18 | Hulin, Bernard; Newton, Linda S.; Cabral, Shawn; Walker, Aaron J.; Bordner, Jon Three-component, stereoselective palladium-catalyzed synthesis of functionalized bicyclopentanoids. Organic letters, 2004, 6, 4343-4345 |
1506941 | CIF | C60 H50 | C 1 2/c 1 | 20.496; 10.883; 20.523 90; 114.23; 90 | 4174.5 | Dai, Weixiang; Petersen, Jeffrey L.; Wang, Kung K. Synthesis and structure of a helical diindenophenanthrene with four congested phenyl substituents as a molecular spiral staircase. Organic letters, 2004, 6, 4355-4357 |
1506942 | CIF | C33 H28 | P b c a | 8.8482; 17.6806; 29.5631 90; 90; 90 | 4624.9 | Dai, Weixiang; Petersen, Jeffrey L.; Wang, Kung K. Synthesis and structure of a helical diindenophenanthrene with four congested phenyl substituents as a molecular spiral staircase. Organic letters, 2004, 6, 4355-4357 |
1506943 | CIF | C18 H22 N O6 V | C 1 2 1 | 34.174; 6.545; 8.939 90; 103.211; 90 | 1946.46 | Chen, Chien-Tien; Lin, Jin-Sheng; Kuo, Jen-Huang; Weng, Shiue-Shien; Cuo, Ting-Shen; Lin, Yi-Wen; Cheng, Chien-Chung; Huang, Yan-Chen; Yu, Jen-Kan; Chou, Pi-Tai Site-selective DNA photocleavage involving unusual photoinitiated tautomerization of chiral tridentate vanadyl(V) complexes derived from N-salicylidene alpha-amino acids. Organic letters, 2004, 6, 4471-4474 |
1506944 | CIF | C19 H24 N O6 V | P 2 21 21 | 6.661; 9.106; 32.605 90; 90; 90 | 1977.66 | Chen, Chien-Tien; Lin, Jin-Sheng; Kuo, Jen-Huang; Weng, Shiue-Shien; Cuo, Ting-Shen; Lin, Yi-Wen; Cheng, Chien-Chung; Huang, Yan-Chen; Yu, Jen-Kan; Chou, Pi-Tai Site-selective DNA photocleavage involving unusual photoinitiated tautomerization of chiral tridentate vanadyl(V) complexes derived from N-salicylidene alpha-amino acids. Organic letters, 2004, 6, 4471-4474 |
1506945 | CIF | C19 H24 N O6 V | P 21 21 2 | 9.521; 32.527; 6.7189 90; 90; 90 | 2080.8 | Chen, Chien-Tien; Lin, Jin-Sheng; Kuo, Jen-Huang; Weng, Shiue-Shien; Cuo, Ting-Shen; Lin, Yi-Wen; Cheng, Chien-Chung; Huang, Yan-Chen; Yu, Jen-Kan; Chou, Pi-Tai Site-selective DNA photocleavage involving unusual photoinitiated tautomerization of chiral tridentate vanadyl(V) complexes derived from N-salicylidene alpha-amino acids. Organic letters, 2004, 6, 4471-4474 |
1506946 | CIF | C22 H22 N O6 V | P 1 21 1 | 11.097; 7.218; 13.391 90; 105.166; 90 | 1035.24 | Chen, Chien-Tien; Lin, Jin-Sheng; Kuo, Jen-Huang; Weng, Shiue-Shien; Cuo, Ting-Shen; Lin, Yi-Wen; Cheng, Chien-Chung; Huang, Yan-Chen; Yu, Jen-Kan; Chou, Pi-Tai Site-selective DNA photocleavage involving unusual photoinitiated tautomerization of chiral tridentate vanadyl(V) complexes derived from N-salicylidene alpha-amino acids. Organic letters, 2004, 6, 4471-4474 |
1506947 | CIF | C10 H10 N2 O2 S | P -1 | 6.36; 7.68; 14.36 89.06; 79.77; 73.49 | 661 | Han, Hoon; Bae, Imhyuck; Yoo, Eun Jeong; Lee, Junseong; Do, Youngkyu; Chang, Sukbok Notable coordination effects of 2-pyridinesulfonamides leading to efficient aziridination and selective aziridine ring opening. Organic letters, 2004, 6, 4109-4112 |
1506948 | CIF | C16 H18 O6 | P 1 21 1 | 8.8086; 8.4239; 11.2036 90; 113.233; 90 | 763.92 | Le, Julie Cong-Dung; Pagenkopf, Brian L. A new class of substituted aryl bis(oxazoline) ligands for highly enantioselective copper-catalyzed asymmetric aldol addition of dienolsilane to pyruvate and glyoxylate esters. Organic letters, 2004, 6, 4097-4099 |
1506949 | CIF | C31 H42 N2 O4 | P 1 21 1 | 10.2344; 9.9456; 15.2225 90; 109.187; 90 | 1463.39 | Le, Julie Cong-Dung; Pagenkopf, Brian L. A new class of substituted aryl bis(oxazoline) ligands for highly enantioselective copper-catalyzed asymmetric aldol addition of dienolsilane to pyruvate and glyoxylate esters. Organic letters, 2004, 6, 4097-4099 |
1506950 | CIF | C27 H43 B F9 N2 O4 P S2 | P 21 21 21 | 10.6312; 13.4978; 24.4697 90; 90; 90 | 3511.3 | Duncan, Andrew P.; Leighton, James L. Enantioselective Cu-catalyzed conjugate addition of diethylzinc to acyclic aliphatic enones. Organic letters, 2004, 6, 4117-4119 |
1506951 | CIF | C12 H18 O5 | P 1 21 1 | 8.6269; 6.722; 10.4529 90; 92.173; 90 | 605.73 | Bravo, 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 | CIF | C11 H17 Br O4 | P 32 2 1 | 7.208; 7.208; 42.0575 90; 90; 120 | 1892.36 | Bravo, 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 | CIF | C56 H34 F24 O3 P2 | P -1 | 12.7183; 15.7674; 16.5468 67.448; 67.65; 71.824 | 2780.2 | Wu, 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 | CIF | C48 H28 F12 O2 P2 | C 1 2/c 1 | 28.7227; 8.4943; 17.9976 90; 109.824; 90 | 4130.8 | Wu, 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 | CIF | C56 H34 F24 O P2 | P -1 | 13.3186; 14.8047; 15.3134 85.932; 72.993; 73.854 | 2773.35 | Wu, 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 | CIF | C48 H28 F12 P2 | C 1 2/c 1 | 28.4224; 8.0575; 18.7865 90; 110.05; 90 | 4041.61 | Wu, 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 | CIF | C30 H41 N3 O8 | C 1 2 1 | 24.287; 5.089; 26.519 90; 103.94; 90 | 3181 | Ray, 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 | CIF | C29 H39 N3 O8 | C 1 2 1 | 24.3; 5.062; 25.97 90; 102.882; 90 | 3114 | Ray, 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 | CIF | C19 H26 N2 O3 S | P 21 21 21 | 6.9465; 13.0021; 20.3093 90; 90; 90 | 1834.32 | Overman, 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 | CIF | C13 H21 N3 O S | P 21 21 21 | 7.9972; 11.8432; 14.5588 90; 90; 90 | 1378.9 | Overman, 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 | CIF | C23 H42 O3 S2 Si | P -1 | 7.323; 17.75; 19.552 81.888; 88.834; 88.885 | 2515.1 | Overman, 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 | CIF | C11 H18 O3 S2 | C 1 2 1 | 14.0471; 7.9277; 11.5877 90; 102.849; 90 | 1258.11 | Overman, 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 | CIF | C23 H32 N2 O3 S3 | C 1 2/c 1 | 61.439; 10.1168; 31.402 90; 97.819; 90 | 19337 | Overman, 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 | CIF | C20 H25 N O6 | P 1 21/c 1 | 12.1406; 13.1539; 12.965 90; 113.258; 90 | 1902.2 | Overman, 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 | CIF | C24 H23 Cl O4 | P 1 21/c 1 | 9.4195; 21.7175; 10.4372 90; 90.8136; 90 | 2134.9 | Babu, 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 | CIF | C20 H20 Br Cl O4 | P 1 21/a 1 | 11.847; 8.94; 19.015 90; 93.27; 90 | 2011 | Babu, 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 | CIF | C17 H19 N O3 S | P 1 21/c 1 | 15.306; 11.1614; 9.8395 90; 94.631; 90 | 1675.5 | Andreana, Peter R.; Liu, Chang C.; Schreiber, Stuart L. Stereochemical control of the Passerini reaction. Organic letters, 2004, 6, 4231-4233 |
1506968 | CIF | C17 H18 Br N O4 | P 21 21 21 | 9.4372; 20.8127; 36.61 90; 90; 90 | 7190.7 | Andreana, Peter R.; Liu, Chang C.; Schreiber, Stuart L. Stereochemical control of the Passerini reaction. Organic letters, 2004, 6, 4231-4233 |
1506969 | CIF | C10 H12 F2 N2 O3 | P 1 21/c 1 | 6.1123; 19.495; 9.2417 90; 107.676; 90 | 1049.2 | Yang, Yan-Yan; Meng, Wei-Dong; Qing, Feng-Ling Synthesis of 2',3'-dideoxy-6',6'-difluorocarbocyclic nucleosides. Organic letters, 2004, 6, 4257-4259 |
1506970 | CIF | C17 H24 N O2 P S | P 41 21 2 | 13.6603; 13.6603; 40.766 90; 90; 90 | 7607.1 | Kobayashi, 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 |
1506971 | CIF | C16 H21 Cl N O2 P S | P 41 21 2 | 13.7121; 13.7121; 40.339 90; 90; 90 | 7584.6 | Kobayashi, 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 |
1506972 | CIF | C16 H21 Br N O2 P S | P 41 21 2 | 13.8231; 13.8231; 39.921 90; 90; 90 | 7628 | Kobayashi, 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 |
1506973 | CIF | C36 H62 Cl2 F12 N8 P2 Pd | P -1 | 9.882; 10.758; 12.086 109.18; 93.91; 106.21 | 1147 | Xiao, Ji-Chang; Twamley, Brendan; Shreeve, Jean'ne M. An ionic liquid-coordinated palladium complex: a highly efficient and recyclable catalyst for the Heck reaction. Organic letters, 2004, 6, 3845-3847 |
1506974 | CIF | C18 H26 F3 N O5 S | P 1 21 1 | 9.6476; 8.9745; 11.493 90; 97.917; 90 | 985.6 | Peelen, Timothy J.; Chi, Yonggui; English, Emily Payne; Gellman, Samuel H. Synthesis of 4,4-disubstituted 2-aminocyclopentanecarboxylic acid derivatives and their incorporation into 12-helical beta-peptides. Organic letters, 2004, 6, 4411-4414 |
1506975 | CIF | C28 H30 F3 N O5 S | P 21 21 21 | 6.4665; 17.5592; 23.0312 90; 90; 90 | 2615.1 | Peelen, Timothy J.; Chi, Yonggui; English, Emily Payne; Gellman, Samuel H. Synthesis of 4,4-disubstituted 2-aminocyclopentanecarboxylic acid derivatives and their incorporation into 12-helical beta-peptides. Organic letters, 2004, 6, 4411-4414 |
1506976 | CIF | C31 H42 Cl N O6 | P 1 21 1 | 7.3611; 36.908; 11.4393 90; 90.954; 90 | 3107.4 | Peelen, Timothy J.; Chi, Yonggui; English, Emily Payne; Gellman, Samuel H. Synthesis of 4,4-disubstituted 2-aminocyclopentanecarboxylic acid derivatives and their incorporation into 12-helical beta-peptides. Organic letters, 2004, 6, 4411-4414 |
1506977 | CIF | C19 H21 F3 O4 S | P 1 21/n 1 | 11.692; 8.756; 18.745 90; 98.724; 90 | 1896.82 | Isobe, Hiroyuki; Sato, Sota; Tanaka, Takatsugu; Tokuyama, Hidetoshi; Nakamura, Eiichi Thermal and palladium-catalyzed [3 + 2] synthesis of cyclopentadienone acetals from cyclopropenone acetals and acetylenes. Organic letters, 2004, 6, 3569-3571 |
1506978 | CIF | C20 H22 O6 | P 21 21 21 | 8.134; 12.218; 18.929 90; 90; 90 | 1881.19 | Isobe, Hiroyuki; Sato, Sota; Tanaka, Takatsugu; Tokuyama, Hidetoshi; Nakamura, Eiichi Thermal and palladium-catalyzed [3 + 2] synthesis of cyclopentadienone acetals from cyclopropenone acetals and acetylenes. Organic letters, 2004, 6, 3569-3571 |
1506979 | CIF | C21 H24 O7 | P 21 21 21 | 6.368; 8.179; 38.824 90; 90; 90 | 2022.1 | Isobe, Hiroyuki; Sato, Sota; Tanaka, Takatsugu; Tokuyama, Hidetoshi; Nakamura, Eiichi Thermal and palladium-catalyzed [3 + 2] synthesis of cyclopentadienone acetals from cyclopropenone acetals and acetylenes. Organic letters, 2004, 6, 3569-3571 |
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