Crystallography Open Database

Result: there are 1037 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)

Searching journal of publication like 'Organic letters' volume of publication is 18

Blue left arrow Blue left arrow First | Blue left arrow Previous 50 | of 21 | Next 50 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1542655 CIFC24 H26 N4 O4P -19.715; 10.003; 13.038
105.483; 98.771; 111.44		1091.5Zhao, Hong-Wu; Li, Bo; Pang, Hai-Liang; Tian, Ting; Chen, Xiao-Qin; Song, Xiu-Qing; Meng, Wei; Yang, Zhao; Zhao, Yu-Di; Liu, Yue-Yang
Diastereoselective 1,3-Dipolar Cycloadditions of N,N'-Cyclic Azomethine Imines with Iminooxindoles for Access to Oxindole Spiro-N,N-bicyclic Heterocycles.
Organic letters, 2016, 18, 848-851
1542656 CIFC20 H11 Cl6 O2 P S2P 1 21/n 111.338; 11.077; 18.981
90; 106.186; 90		2289.4Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542657 CIFC18 H9 O3 P SP 1 21/n 18.3936; 15.6127; 10.697
90; 100.496; 90		1378.35Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542658 CIFC18 H9 P S3P -13.9829; 10.6559; 17.2702
86.043; 89.121; 81.767		723.68Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542659 CIFC18 H9 O2 P SP c c n16.762; 22.071; 7.4782
90; 90; 90		2766.6Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542660 CIFC21 H16 F2 N O4 P SP 1 21/c 111.099; 11.479; 14.854
90; 95.89; 90		1882.5Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542661 CIFC18 H9 O P S3P 1 21/n 19.166; 10.699; 15.212
90; 101.527; 90		1461.7Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542662 CIFC18 H9 O P S2P b c a8.0119; 20.775; 34.265
90; 90; 90		5703.3Yamamura, Masaki; Hasegawa, Toru; Nabeshima, Tatsuya
Synthesis of Phosphorus-Centered and Chalcogen-Bridged Concave Molecules: Modulation of Bowl Geometries and Packing Structures by Changing Bridging Atoms.
Organic letters, 2016, 18, 816-819
1542663 CIFC30 H28 N O3 PP 1 21/c 18.675; 19.74; 15.454
90; 106.49; 90		2538Jiang, Jin; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Diethyl Phosphite Initiated Coupling of α-Ketoesters with Imines for Synthesis of α-Phosphonyloxy-β-amino Acid Derivatives and Aziridine-2-carboxylates.
Organic letters, 2016, 18, 880-883
1542664 CIFC29 H36 N O9 P SP 1 21/a 116.58; 10.731; 17.82
90; 104.369; 90		3071Jiang, Jin; Liu, Hui; Lu, Chong-Dao; Xu, Yan-Jun
Diethyl Phosphite Initiated Coupling of α-Ketoesters with Imines for Synthesis of α-Phosphonyloxy-β-amino Acid Derivatives and Aziridine-2-carboxylates.
Organic letters, 2016, 18, 880-883
1542665 CIFC19 H26 Cl3 N2 RhP 1 21/c 111.0944; 14.838; 13.848
90; 105.603; 90		2195.6Qi, Zisong; Yu, Songjie; Li, Xingwei
Rh(III)-Catalyzed Synthesis of N-Unprotected Indoles from Imidamides and Diazo Ketoesters via C-H Activation and C-C/C-N Bond Cleavage.
Organic letters, 2016, 18, 700-703
1542666 CIFC17 H13 Br N2 O2P 1 21/c 14.4677; 16.8234; 20.1968
90; 92.566; 90		1516.51Ma, Haichao; Li, Dianjun; Yu, Wei
Synthesis of Quinoxaline Derivatives via Tandem Oxidative Azidation/Cyclization Reaction of N-Arylenamines.
Organic letters, 2016, 18, 868-871
1542667 CIFC26 H34 O8P 21 21 217.8754; 9.4243; 32.1424
90; 90; 90		2385.61Wan, Luo-Sheng; Shao, Li-Dong; Fu, Liangbing; Xu, Jun; Zhu, Guo-Lei; Peng, Xing-Rong; Li, Xiao-Nian; Li, Yan; Qiu, Ming-Hua
One-Step Semisynthesis of a Segetane Diterpenoid from a Jatrophane Precursor via a Diels-Alder Reaction.
Organic letters, 2016, 18, 496-499
1542668 CIFC42 H32 SP -18.317; 16.04; 23.373
108.62; 98.945; 90.295		2913.9Bhanuchandra, M.; Yorimitsu, Hideki; Osuka, Atsuhiro
Synthesis of Spirocyclic Diarylfluorenes by One-Pot Twofold SNAr Reactions of Diaryl Sulfones with Diarylmethanes.
Organic letters, 2016, 18, 384-387
1542669 CIFC26 H15 F3 SP -17.4947; 10.4244; 12.3741
83; 82.694; 81.603		943.36Bhanuchandra, M.; Yorimitsu, Hideki; Osuka, Atsuhiro
Synthesis of Spirocyclic Diarylfluorenes by One-Pot Twofold SNAr Reactions of Diaryl Sulfones with Diarylmethanes.
Organic letters, 2016, 18, 384-387
1542670 CIFC24 H32 N2 O3 SP 1 21 116.9083; 5.97938; 23.1232
90; 103.885; 90		2269.47Yoshizaki, Soichi; Nakamura, Yu; Masutomi, Koji; Yoshida, Tomoka; Noguchi, Keiichi; Shibata, Yu; Tanaka, Ken
Rhodium-Catalyzed Asymmetric [2 + 2 + 2] Cycloaddition of 1,6-Enynes with Cyclopropylideneacetamides.
Organic letters, 2016, 18, 388-391
1542671 CIFC28 H20 N2 O6 SP b c a13.7519; 14.9993; 22.6562
90; 90; 90		4673.27Kumar, N. N. Bhuvan; Kutateladze, Andrei G.
Photoassisted Diversity-Oriented Synthesis: Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxazole Pendants, and Subsequent Postphotochemical Multicomponent Modifications.
Organic letters, 2016, 18, 460-463
1542672 CIFC17 H14 N2 O4P 1 21/n 19.1645; 8.7385; 18.3694
90; 104.426; 90		1424.71Kumar, N. N. Bhuvan; Kutateladze, Andrei G.
Photoassisted Diversity-Oriented Synthesis: Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxazole Pendants, and Subsequent Postphotochemical Multicomponent Modifications.
Organic letters, 2016, 18, 460-463
1542673 CIFC19 H13 Cl N2 O3C 1 2/c 117.6228; 12.8352; 14.1014
90; 91.786; 90		3188.08Kumar, N. N. Bhuvan; Kutateladze, Andrei G.
Photoassisted Diversity-Oriented Synthesis: Intramolecular Cycloadditions of Photogenerated Azaxylylenes with Oxazole Pendants, and Subsequent Postphotochemical Multicomponent Modifications.
Organic letters, 2016, 18, 460-463
1542674 CIFC36 H50 S4 Si2P -112.2329; 17.7221; 19.3408
69.034; 72.015; 72.867		3643.1Chang, Shao-Ling; Lu, Chih-Wen; Lai, Yu-Ying; Hsu, Jhih-Yang; Cheng, Yen-Ju
Synthesis and Molecular Properties of Two Isomeric Dialkylated Tetrathienonaphthalenes.
Organic letters, 2016, 18, 368-371
1542675 CIFC34 H44 S4 Si2P -111.715; 12.209; 15.564
76.856; 75.796; 79.474		2082.4Chang, Shao-Ling; Lu, Chih-Wen; Lai, Yu-Ying; Hsu, Jhih-Yang; Cheng, Yen-Ju
Synthesis and Molecular Properties of Two Isomeric Dialkylated Tetrathienonaphthalenes.
Organic letters, 2016, 18, 368-371
1542676 CIFC24 H18 O3P 1 21/n 19.9595; 12.5319; 14.6208
90; 97.484; 90		1809.3More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542677 CIFC16 H12 O3P -17.6359; 8.6199; 10.087
80.935; 79.666; 69.242		607.6More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542678 CIFC19 H18 O4P 1 21/c 19.4895; 8.7747; 19.062
90; 101.174; 90		1557.2More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542679 CIFC17 H14 O3P 1 21/n 19.3485; 13.5764; 10.5947
90; 101.444; 90		1317.94More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542680 CIFC16 H12 O3P b c a10.0417; 18.527; 26.755
90; 90; 90		4977.6More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542681 CIFC22 H22 O5P -19.3342; 10.9832; 19.0771
103.527; 91.081; 99.292		1873.3More, Atul A.; Ramana, Chepuri V.
o-Quinone Methides via Oxone-Mediated Benzofuran Oxidative Dearomatization and Their Intramolecular Cycloaddition with Carbonyl Groups: An Expeditious Construction of the Central Tetracyclic Core of Integrastatins, Epicoccolide A, and Epicocconigrone A.
Organic letters, 2016, 18, 612-615
1542682 CIFC12 H11 Cl F3 N OP 1 21/n 110.761; 5.854; 19.673
90; 102.693; 90		1209Fu, Mingyang; Chen, Long; Jiang, Yongpeng; Jiang, Zhong-Xing; Yang, Zhigang
Copper-Catalyzed Intermolecular Chloro- and Bromotrifluoromethylation of Alkenes.
Organic letters, 2016, 18, 348-351
1542683 CIFC36 H36 Br N2 O4.5 SC 1 2 127.2716; 10.7113; 11.2422
90; 90.5644; 90		3283.85Wang, Shoulei; Rodriguez-Escrich, Carles; Pericàs, Miquel A
H-Bond-Directing Organocatalyst for Enantioselective [4 + 2] Cycloadditions via Dienamine Catalysis.
Organic letters, 2016, 18, 556-559
1542684 CIFC13 H10 N2 SP -13.9105; 10.8964; 12.403
97.328; 94.957; 92.265		521.54Sharma, Shivani; Pathare, Ramdas S.; Maurya, Antim K.; Gopal, Kandasamy; Roy, Tapta Kanchan; Sawant, Devesh M.; Pardasani, Ram T.
Ruthenium Catalyzed Intramolecular C-S Coupling Reactions: Synthetic Scope and Mechanistic Insight.
Organic letters, 2016, 18, 356-359
1542685 CIFC14 H12 N2 O SP 1 21/c 113.1514; 12.8014; 7.2224
90; 105.094; 90		1173.99Sharma, Shivani; Pathare, Ramdas S.; Maurya, Antim K.; Gopal, Kandasamy; Roy, Tapta Kanchan; Sawant, Devesh M.; Pardasani, Ram T.
Ruthenium Catalyzed Intramolecular C-S Coupling Reactions: Synthetic Scope and Mechanistic Insight.
Organic letters, 2016, 18, 356-359
1542686 CIFC26 H22 Cl2 N2 O4P 1 21/c 19.921; 17.9238; 12.9555
90; 90.022; 90		2303.8Zhou, Yunfei; Zhu, Jianming; Li, Bo; Zhang, Yong; Feng, Jia; Hall, Adrian; Shi, Jiye; Zhu, Weiliang
Access to Different Isomeric Dibenzoxazepinones through Copper-Catalyzed C-H Etherification and C-N Bond Construction with Controllable Smiles Rearrangement.
Organic letters, 2016, 18, 380-383
1542687 CIFC24 H17 Cl N2 O3P 1 21/c 114.8316; 16.4395; 7.8011
90; 93.277; 90		1898.99Zhou, Yunfei; Zhu, Jianming; Li, Bo; Zhang, Yong; Feng, Jia; Hall, Adrian; Shi, Jiye; Zhu, Weiliang
Access to Different Isomeric Dibenzoxazepinones through Copper-Catalyzed C-H Etherification and C-N Bond Construction with Controllable Smiles Rearrangement.
Organic letters, 2016, 18, 380-383
1542688 CIFC32 H16 Br8 O8C 1 2/c 121.0972; 15.0686; 14.2085
90; 128.249; 90		3547.3Kumar, Yogendra; Kumar, Sharvan; Kumar Keshri, Sudhir; Shukla, Jyoti; Singh, Shiv Shankar; Thakur, Tejender S.; Denti, Mitchell; Facchetti, Antonio; Mukhopadhyay, Pritam
Synthesis of Octabromoperylene Dianhydride and Diimides: Evidence of Halogen Bonding and Semiconducting Properties.
Organic letters, 2016, 18, 472-475
1542689 CIFC11 H10 N4 O3P b c a10.487; 13.0919; 16.145
90; 90; 90		2216.6Pawar, Govind Goroba; Brahmanandan, Abhilashamole; Kapur, Manmohan
Palladium(II)-Catalyzed, Heteroatom-Directed, Regioselective C-H Nitration of Anilines Using Pyrimidine as a Removable Directing Group.
Organic letters, 2016, 18, 448-451
1542690 CIFC34 H35 Br N2 OP 21 21 2110.839; 23.282; 24.36
90; 90; 90		6147Li, Xuanyi; Xu, Xiuyan; Wei, Weiwei; Lin, Aijun; Yao, Hequan
Organocatalyzed Asymmetric 1,6-Conjugate Addition of para-Quinone Methides with Dicyanoolefins.
Organic letters, 2016, 18, 428-431
1542691 CIFC14 H17 F N2 O2 SP 1 21 15.8834; 11.064; 11.101
90; 102.611; 90		705.2Hajra, Saumen; Aziz, Sk Mohammad; Jana, Bibekananda; Mahish, Prosenjit; Das, Dhiraj
Synthesis of Chiral Spiro-Aziridine Oxindoles via Aza-Corey-Chaykovsky Reaction of Isatin Derived N-tert-Butanesulfinyl Ketimines.
Organic letters, 2016, 18, 532-535
1542692 CIFC32 H31 N O5P 1 21/c 110.3073; 11.8581; 21.8138
90; 94.816; 90		2656.8Gao, Fei; Yang, Chao; Ma, Na; Gao, Guo-Lin; Li, Dazhi; Xia, Wujiong
Visible-Light-Mediated 1,7-Enyne Bicyclizations for Synthesis of Cyclopenta[c]quinolines and Benzo[j]phenanthridines.
Organic letters, 2016, 18, 600-603
1542693 CIFC26 H20 F3 N OI 1 2/a 118.3718; 5.6809; 40.089
90; 100.975; 90		4107.5Gao, Fei; Yang, Chao; Ma, Na; Gao, Guo-Lin; Li, Dazhi; Xia, Wujiong
Visible-Light-Mediated 1,7-Enyne Bicyclizations for Synthesis of Cyclopenta[c]quinolines and Benzo[j]phenanthridines.
Organic letters, 2016, 18, 600-603
1542694 CIFC29 H25 F2 N O3P -110.2357; 10.5168; 12.7893
71.454; 71.195; 73.002		1207.61Gao, Fei; Yang, Chao; Ma, Na; Gao, Guo-Lin; Li, Dazhi; Xia, Wujiong
Visible-Light-Mediated 1,7-Enyne Bicyclizations for Synthesis of Cyclopenta[c]quinolines and Benzo[j]phenanthridines.
Organic letters, 2016, 18, 600-603
1542695 CIFC18 H24 O3P 21 21 217.8269; 8.7254; 23.407
90; 90; 90		1598.5Liu, Chenguang; Zeng, Zhixiong; Chen, Renzhi; Jiang, Xunjin; Wang, Yinglu; Zhang, Yandong
Total Synthesis of (+)-Fusarisetin A Driven by a One-Pot Four-Reaction Process.
Organic letters, 2016, 18, 624-627
1542696 CIFC18 H12 Br2 O2 SP -17.9582; 8.0654; 13.665
82.257; 84.908; 72.622		828.3Wang, Miao; Xiang, Jia-Chen; Cheng, Yan; Wu, Yan-Dong; Wu, An-Xin
Synthesis of 2,4,5-Trisubstituted Furans via a Triple C(sp(3))-H Functionalization Reaction Using Rongalite as the C1 Unit.
Organic letters, 2016, 18, 524-527
1542697 CIFC19 H16 O4 S2P -17.573; 8.012; 15.475
77.359; 78.217; 86.315		896.7Wang, Miao; Xiang, Jia-Chen; Cheng, Yan; Wu, Yan-Dong; Wu, An-Xin
Synthesis of 2,4,5-Trisubstituted Furans via a Triple C(sp(3))-H Functionalization Reaction Using Rongalite as the C1 Unit.
Organic letters, 2016, 18, 524-527
1542698 CIFC23.5 H14.5 Cl4.5 N3 O8P -19.645; 11.531; 23.18
92.059; 90.249; 95.534		2564.25Yoon, Ina; Suh, Sung-Eun; Barros, Stephanie A.; Chenoweth, David M.
Synthesis of 9-Substituted Triptycene Building Blocks for Solid-Phase Diversification and Nucleic Acid Junction Targeting.
Organic letters, 2016, 18, 1096
1542699 CIFC17 H16 F N OP -15.5492; 10.9097; 11.6094
102.644; 93.799; 96.078		679.03Wang, Yi-Feng; Hu, Ming; Hayashi, Hirohito; Xing, Bengang; Chiba, Shunsuke
Linking of Alcohols with Vinyl Azides.
Organic letters, 2016, 18, 992
1542700 CIFC22 H17 Cl2 F3 N2 O3P 21 21 217.6378; 15.9147; 18.2712
90; 90; 90		2220.9Li, Xiaoyuan; Su, Jinhuan; Liu, Zhourujun; Zhu, Yuanyuan; Dong, Zhenghao; Qiu, Shuai; Wang, Jiayi; Lin, Li; Shen, Zhiqiang; Yan, Wenjin; Wang, Kairong; Wang, Rui
Synthesis of Chiral α-Trifluoromethylamines with 2,2,2-Trifluoroethylamine as a "Building Block".
Organic letters, 2016, 18, 956
1542701 CIFC26 H20 Cl F3 N2 O3P 1 21 110.2811; 11.149; 11.3115
90; 115.56; 90		1169.7Li, Xiaoyuan; Su, Jinhuan; Liu, Zhourujun; Zhu, Yuanyuan; Dong, Zhenghao; Qiu, Shuai; Wang, Jiayi; Lin, Li; Shen, Zhiqiang; Yan, Wenjin; Wang, Kairong; Wang, Rui
Synthesis of Chiral α-Trifluoromethylamines with 2,2,2-Trifluoroethylamine as a "Building Block".
Organic letters, 2016, 18, 956
1542702 CIFC10 H6 F3 N3 OP -17.0244; 7.2782; 10.394
99.34; 92.323; 91.732		523.55Pieber, Bartholomäus; Kappe, C. Oliver
Generation and Synthetic Application of Trifluoromethyl Diazomethane Utilizing Continuous Flow Technologies.
Organic letters, 2016, 18, 1076
1542703 CIFC16 H15 F5 O3 SP -15.584; 11.7071; 12.0947
85.184; 83.294; 87.881		782.18Friese, Florian W.; Dreier, Anna-Lena; Matsnev, Andrej V.; Daniliuc, Constantin G.; Thrasher, Joseph S.; Haufe, Günter
Anti-Selective Aldol Reactions of Pentafluorosulfanylacetic Acid Esters with Aldehydes Mediated by Dicyclohexylchloroborane.
Organic letters, 2016, 18, 1012
1542704 CIFC17 H23 Cl2 F5 O3 SP -110.0879; 13.4704; 16.5159
66.318; 85.001; 89.698		2046.4Friese, Florian W.; Dreier, Anna-Lena; Matsnev, Andrej V.; Daniliuc, Constantin G.; Thrasher, Joseph S.; Haufe, Günter
Anti-Selective Aldol Reactions of Pentafluorosulfanylacetic Acid Esters with Aldehydes Mediated by Dicyclohexylchloroborane.
Organic letters, 2016, 18, 1012

Blue left arrow Blue left arrow First | Blue left arrow Previous 50 | of 21 | Next 50 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!
Top of the page
All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.