Crystallography Open Database
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Searching journal of publication like 'Organic letters' volume of publication is 16
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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1516152 | CIF | C16 H13 Br O3 | P 1 21 1 | 7.952; 12.184; 14.721 90; 92.596; 90 | 1424.8 | Fu, Liangbing; Wang, Hengbin; Davies, Huw M. L. Role of Ortho-Substituents on Rhodium-Catalyzed Asymmetric Synthesis of β-Lactones by Intramolecular C-H Insertions of Aryldiazoacetates. Organic letters, 2014, 16, 3036-3039 |
1516153 | CIF | C11 H11 Br O3 | P 21 21 21 | 12.06; 12.066; 14.641 90; 90; 90 | 2130.5 | Fu, Liangbing; Wang, Hengbin; Davies, Huw M. L. Role of Ortho-Substituents on Rhodium-Catalyzed Asymmetric Synthesis of β-Lactones by Intramolecular C-H Insertions of Aryldiazoacetates. Organic letters, 2014, 16, 3036-3039 |
1516154 | CIF | C10 H9 Br O3 | P 1 21 1 | 6.2085; 5.3383; 15.239 90; 95.715; 90 | 502.6 | Fu, Liangbing; Wang, Hengbin; Davies, Huw M. L. Role of Ortho-Substituents on Rhodium-Catalyzed Asymmetric Synthesis of β-Lactones by Intramolecular C-H Insertions of Aryldiazoacetates. Organic letters, 2014, 16, 3036-3039 |
1516169 | CIF | C10 H8 B2 F4 N4 | C 1 2/m 1 | 12.2662; 6.8136; 7.0499 90; 105.816; 90 | 566.9 | Yu, Changjiang; Jiao, Lijuan; Zhang, Ping; Feng, Zeya; Cheng, Chi; Wei, Yun; Mu, Xiaolong; Hao, Erhong Highly Fluorescent BF2 Complexes of Hydrazine-Schiff Base Linked Bispyrrole. Organic letters, 2014, 16, 3048-3051 |
1516170 | CIF | C14 H16 B2 F4 N4 | P 1 21/c 1 | 9.2147; 12.1024; 7.3238 90; 108.772; 90 | 773.3 | Yu, Changjiang; Jiao, Lijuan; Zhang, Ping; Feng, Zeya; Cheng, Chi; Wei, Yun; Mu, Xiaolong; Hao, Erhong Highly Fluorescent BF2 Complexes of Hydrazine-Schiff Base Linked Bispyrrole. Organic letters, 2014, 16, 3048-3051 |
1516171 | CIF | C18 H24 B2 F4 N4 | P 1 21/n 1 | 9.676; 13.659; 15.313 90; 103.66; 90 | 1966.6 | Yu, Changjiang; Jiao, Lijuan; Zhang, Ping; Feng, Zeya; Cheng, Chi; Wei, Yun; Mu, Xiaolong; Hao, Erhong Highly Fluorescent BF2 Complexes of Hydrazine-Schiff Base Linked Bispyrrole. Organic letters, 2014, 16, 3048-3051 |
1516172 | CIF | C10 H9 B F2 N4 | P b c a | 12.306; 9.48; 18.766 90; 90; 90 | 2189.3 | Yu, Changjiang; Jiao, Lijuan; Zhang, Ping; Feng, Zeya; Cheng, Chi; Wei, Yun; Mu, Xiaolong; Hao, Erhong Highly Fluorescent BF2 Complexes of Hydrazine-Schiff Base Linked Bispyrrole. Organic letters, 2014, 16, 3048-3051 |
1516173 | CIF | C14 H17 B F2 N4 | P 1 21/c 1 | 8.058; 21.225; 8.7995 90; 102.217; 90 | 1470.9 | Yu, Changjiang; Jiao, Lijuan; Zhang, Ping; Feng, Zeya; Cheng, Chi; Wei, Yun; Mu, Xiaolong; Hao, Erhong Highly Fluorescent BF2 Complexes of Hydrazine-Schiff Base Linked Bispyrrole. Organic letters, 2014, 16, 3048-3051 |
1516174 | CIF | C26 H22 F6 N4 O4 | C 1 2/c 1 | 29.895; 12.375; 15.464 90; 107.104; 90 | 5468 | Zhang, Fa-Guang; Wei, Yi; Yi, Yu-Ping; Nie, Jing; Ma, Jun-An Regioselective Cycloaddition of Trifluorodiazoethane with Electron-Deficient Allenic Esters and Ketones: Access to CF3-Substituted Pyrazolines and Pyrazoles. Organic letters, 2014, 16, 3122-3125 |
1516175 | CIF | C15 H18 N2 O3 | P 1 21/n 1 | 9.4197; 8.3092; 17.992 90; 98.7; 90 | 1392 | Cai, Shangjun; Chen, Chao; Shao, Peng; Xi, Chanjuan Rh(III)-Catalyzed Cascade Oxidative Olefination/Cyclization of Picolinamides and Alkenes via C-H Activation. Organic letters, 2014, 16, 3142-3145 |
1516176 | CIF | C14 H16 N2 O3 | P 1 21/c 1 | 7.5875; 21.568; 8.3245 90; 110.26; 90 | 1278 | Cai, Shangjun; Chen, Chao; Shao, Peng; Xi, Chanjuan Rh(III)-Catalyzed Cascade Oxidative Olefination/Cyclization of Picolinamides and Alkenes via C-H Activation. Organic letters, 2014, 16, 3142-3145 |
1516232 | CIF | C82.5 H44 F15 N O | P -1 | 14.729; 15.302; 17.015 110.482; 91.5392; 117.76 | 3094.5 | Chou, Chih-Ming; Saito, Shohei; Yamaguchi, Shigehiro Heterotriangulenes π-Expanded at Bridging Positions. Organic letters, 2014, 16, 2868-2871 |
1516233 | CIF | C122.4 H59 Cl3.4 F15 N | P -1 | 26.3661; 26.5069; 39.8191 100.01; 99.1855; 99.1177 | 26552.9 | Chou, Chih-Ming; Saito, Shohei; Yamaguchi, Shigehiro Heterotriangulenes π-Expanded at Bridging Positions. Organic letters, 2014, 16, 2868-2871 |
1516234 | CIF | C78 H32 F15 N | C 1 2/c 1 | 25.7374; 16.733; 30.152 90; 114.227; 90 | 11841.7 | Chou, Chih-Ming; Saito, Shohei; Yamaguchi, Shigehiro Heterotriangulenes π-Expanded at Bridging Positions. Organic letters, 2014, 16, 2868-2871 |
1516235 | CIF | C13 H16 O6 | P b c a | 11.5879; 11.617; 19.7761 90; 90; 90 | 2662.19 | Rout, Saroj Kumar; Guin, Srimanta; Ali, Wajid; Gogoi, Anupal; Patel, Bhisma K. Copper-Catalyzed Esterification of Alkylbenzenes with Cyclic Ethers and Cycloalkanes via C(sp(3))-H Activation Following Cross-Dehydrogenative Coupling. Organic letters, 2014, 16, 3086-3089 |
1516236 | CIF | C49 H36 O5 | P 1 2/n 1 | 9.772; 12.0351; 17.3162 90; 93.947; 90 | 2031.68 | Nandakumar, Meganathan; Karunakaran, Jayachandran; Mohanakrishnan, Arasambattu K. Diels-Alder Reaction of 1,3-Diarylbenzo[c]furans with Thiophene S,S-Dioxide/Indenone Derivatives: A Facile Preparation of Substituted Dibenzothiophene S,S-Dioxides and Fluorenones. Organic letters, 2014, 16, 3068-3071 |
1516237 | CIF | C34 H24 O4 S | P -1 | 13.7369; 13.8077; 16.4824 78.442; 68.211; 80.216 | 2828.35 | Nandakumar, Meganathan; Karunakaran, Jayachandran; Mohanakrishnan, Arasambattu K. Diels-Alder Reaction of 1,3-Diarylbenzo[c]furans with Thiophene S,S-Dioxide/Indenone Derivatives: A Facile Preparation of Substituted Dibenzothiophene S,S-Dioxides and Fluorenones. Organic letters, 2014, 16, 3068-3071 |
1516238 | CIF | C28 H18 O2 S | P 1 21/n 1 | 9.9374; 16.1534; 13.053 90; 100.308; 90 | 2061.49 | Nandakumar, Meganathan; Karunakaran, Jayachandran; Mohanakrishnan, Arasambattu K. Diels-Alder Reaction of 1,3-Diarylbenzo[c]furans with Thiophene S,S-Dioxide/Indenone Derivatives: A Facile Preparation of Substituted Dibenzothiophene S,S-Dioxides and Fluorenones. Organic letters, 2014, 16, 3068-3071 |
1516262 | CIF | C20 H38 Au Cl4 N5 | P -1 | 8.9016; 12.934; 13.6174 63.626; 78.563; 80.061 | 1370.35 | Mirabdolbaghi, Roya; Dudding, Travis; Stamatatos, Theocharis A Class of Phase-Transfer Catalyst with Interionic Strain: Insight into the Bonding of Disubstituted N- vs Carbene-Stabilized N(I)-Centered Cations. Organic letters, 2014, 16, 2790-2793 |
1516263 | CIF | C26 H41 Cl F9 N5 O6 | P 1 21/c 1 | 16.646; 22.121; 9.329 90; 90.328; 90 | 3435.1 | Mirabdolbaghi, Roya; Dudding, Travis; Stamatatos, Theocharis A Class of Phase-Transfer Catalyst with Interionic Strain: Insight into the Bonding of Disubstituted N- vs Carbene-Stabilized N(I)-Centered Cations. Organic letters, 2014, 16, 2790-2793 |
1516264 | CIF | C24 H25 Cl N2 O4 | P 21 21 21 | 11.939; 12.451; 15.057 90; 90; 90 | 2238.3 | Zhang, Han-Ming; Gao, Zhong-Hua; Ye, Song Bifunctional N-Heterocyclic Carbene-Catalyzed Highly Enantioselective Synthesis of Spirocyclic Oxindolo-β-lactams. Organic letters, 2014, 16, 3079-3081 |
1516265 | CIF | C24 H16 N2 O | P b c a | 14.7042; 8.8119; 27.6407 90; 90; 90 | 3581.46 | Dong, Jiaxing; Wang, Fei; You, Jingsong Copper-Mediated Tandem Oxidative C(sp(2))-H/C(sp)-H Alkynylation and Annulation of Arenes with Terminal Alkynes. Organic letters, 2014, 16, 2884-2887 |
1516325 | CIF | C9 H10 N O3 P | P 1 21/n 1 | 6.877; 16.165; 8.684 90; 107.06; 90 | 922.9 | Kim, Yea Rin; Cho, Seungyoon; Lee, Phil Ho Metal-Free Azaphosphaannulation of Phosphonamides through Intramolecular Oxidative C-N Bond Formation. Organic letters, 2014, 16, 3098-3101 |
1516326 | CIF | C10 H12 N O3 P | P 1 21/c 1 | 7.203; 8.501; 17.051 90; 90.9; 90 | 1044 | Kim, Yea Rin; Cho, Seungyoon; Lee, Phil Ho Metal-Free Azaphosphaannulation of Phosphonamides through Intramolecular Oxidative C-N Bond Formation. Organic letters, 2014, 16, 3098-3101 |
1516339 | CIF | C12 H15 N O3 | P 1 21 1 | 8.4867; 6.5654; 11.1325 90; 108.878; 90 | 586.92 | Gietter, Amber A. S.; Gildner, Peter G.; Cinderella, Andrew P.; Watson, Donald A. General Route for Preparing β-Nitrocarbonyl Compounds Using Copper Thermal Redox Catalysis. Organic letters, 2014, 16, 3166-3169 |
1516340 | CIF | C7 H11 N O4 | P 21 21 21 | 5.8815; 8.9902; 15.9025 90; 90; 90 | 840.86 | Gietter, Amber A. S.; Gildner, Peter G.; Cinderella, Andrew P.; Watson, Donald A. General Route for Preparing β-Nitrocarbonyl Compounds Using Copper Thermal Redox Catalysis. Organic letters, 2014, 16, 3166-3169 |
1516341 | CIF | C14 H29 Cl N2 O3 | P 1 21/c 1 | 8.9297; 13.194; 14.536 90; 98.9222; 90 | 1691.89 | Gietter, Amber A. S.; Gildner, Peter G.; Cinderella, Andrew P.; Watson, Donald A. General Route for Preparing β-Nitrocarbonyl Compounds Using Copper Thermal Redox Catalysis. Organic letters, 2014, 16, 3166-3169 |
1516342 | CIF | C14 H17 Cl2 N2 O3 | P 1 21/c 1 | 14.922; 11.523; 9.548 90; 98.829; 90 | 1622 | Gietter, Amber A. S.; Gildner, Peter G.; Cinderella, Andrew P.; Watson, Donald A. General Route for Preparing β-Nitrocarbonyl Compounds Using Copper Thermal Redox Catalysis. Organic letters, 2014, 16, 3166-3169 |
1516343 | CIF | C19 H24 N2 O2 | P 1 21/c 1 | 13.7462; 11.9167; 12.602 90; 106.292; 90 | 1981.4 | Tian, Jingjing; Du, Qiuchen; Guo, Rui; Li, Yun; Cheng, Bin; Zhai, Hongbin Total synthesis of indole alkaloid (±)-subincanadine e. Organic letters, 2014, 16, 3173-3175 |
1516457 | CIF | C14 H19 N O2 S | P 1 21 1 | 7.3662; 17.2624; 11.3119 90; 107.957; 90 | 1368.33 | Hirner, Sebastian; Kolb, Andreas; Westmeier, Johannes; Gebhardt, Sandra; Middel, Stephen; Harms, Klaus; von Zezschwitz, Paultheo Rhodium-catalyzed enantioselective addition of organoaluminum reagents to N-tosyl ketimines. Organic letters, 2014, 16, 3162-3165 |
1516458 | CIF | C15 H21 N O2 S | P 21 21 21 | 7.6766; 17.0877; 22.6809 90; 90; 90 | 2975.2 | Hirner, Sebastian; Kolb, Andreas; Westmeier, Johannes; Gebhardt, Sandra; Middel, Stephen; Harms, Klaus; von Zezschwitz, Paultheo Rhodium-catalyzed enantioselective addition of organoaluminum reagents to N-tosyl ketimines. Organic letters, 2014, 16, 3162-3165 |
1516459 | CIF | C19 H21 N O2 S | P 21 21 21 | 9.7947; 9.9666; 16.9986 90; 90; 90 | 1659.4 | Hirner, Sebastian; Kolb, Andreas; Westmeier, Johannes; Gebhardt, Sandra; Middel, Stephen; Harms, Klaus; von Zezschwitz, Paultheo Rhodium-catalyzed enantioselective addition of organoaluminum reagents to N-tosyl ketimines. Organic letters, 2014, 16, 3162-3165 |
1516460 | CIF | C15 H23 N O2 S | P 1 21 1 | 10.2019; 13.2716; 11.3946 90; 100.893; 90 | 1515 | Hirner, Sebastian; Kolb, Andreas; Westmeier, Johannes; Gebhardt, Sandra; Middel, Stephen; Harms, Klaus; von Zezschwitz, Paultheo Rhodium-catalyzed enantioselective addition of organoaluminum reagents to N-tosyl ketimines. Organic letters, 2014, 16, 3162-3165 |
1516461 | CIF | C29 H23 N5 O2 S | P -1 | 9.4716; 10.8769; 11.9856 83.113; 83.385; 87.083 | 1216.8 | Tokimizu, Yusuke; Oishi, Shinya; Fujii, Nobutaka; Ohno, Hiroaki Gold-Catalyzed Cascade Cyclization of (Azido)ynamides: An Efficient Strategy for the Construction of Indoloquinolines. Organic letters, 2014, 16, 3138-3141 |
1516462 | CIF | C29 H22 N2 O2 S | P b c a | 19.6725; 18.2791; 12.5149 90; 90; 90 | 4500.3 | Tokimizu, Yusuke; Oishi, Shinya; Fujii, Nobutaka; Ohno, Hiroaki Gold-Catalyzed Cascade Cyclization of (Azido)ynamides: An Efficient Strategy for the Construction of Indoloquinolines. Organic letters, 2014, 16, 3138-3141 |
1516464 | CIF | C26 H30 Cl N2 O4 | C 1 2 1 | 21.651; 8.9952; 13.072 90; 92.662; 90 | 2543.1 | Xu, Jianfeng; Mou, Chengli; Zhu, Tingshun; Song, Bao-An; Chi, Yonggui Robin N-heterocyclic carbene-catalyzed chemoselective cross-aza-benzoin reaction of enals with isatin-derived ketimines: access to chiral quaternary aminooxindoles. Organic letters, 2014, 16, 3272-3275 |
1516477 | CIF | C18 H18 Br N O4 S | P 1 21/c 1 | 12.50619; 11.55718; 12.58675 90; 97.3759; 90 | 1804.19 | Medina, Florian; Besnard, Céline; Lacour, Jérôme One-Step Synthesis of Nitrogen-Containing Medium-Sized Rings via α-Imino Diazo Intermediates. Organic letters, 2014, 16, 3232-3235 |
1516478 | CIF | C17 H16 Br N O4 S | P 1 21/a 1 | 12.4111; 11.2306; 12.7572 90; 98.363; 90 | 1759.24 | Medina, Florian; Besnard, Céline; Lacour, Jérôme One-Step Synthesis of Nitrogen-Containing Medium-Sized Rings via α-Imino Diazo Intermediates. Organic letters, 2014, 16, 3232-3235 |
1516499 | CIF | C38 H36 P2 S2 | P 1 21/c 1 | 10.201; 19.08; 16.886 90; 98.7827; 90 | 3248 | Furukawa, Shunsuke; Haga, Shunsuke; Kobayashi, Junji; Kawashima, Takayuki Synthesis of π-Extended Dibenzophospholes by Intramolecular Radical Cyclization and Their Properties. Organic letters, 2014, 16, 3228-3231 |
1516500 | CIF | C38 H36 P2 S2 | P -1 | 9.151; 12.814; 15.408 109.378; 91.446; 107.726 | 1607.4 | Furukawa, Shunsuke; Haga, Shunsuke; Kobayashi, Junji; Kawashima, Takayuki Synthesis of π-Extended Dibenzophospholes by Intramolecular Radical Cyclization and Their Properties. Organic letters, 2014, 16, 3228-3231 |
1516501 | CIF | C23 H23 N O6 | P 21 21 21 | 7.4232; 16.138; 16.7378 90; 90; 90 | 2005.11 | Xiao, You-Cai; Yue, Cai-Zhen; Chen, Peng-Qiao; Chen, Ying-Chun Asymmetric Dearomatic Diels-Alder Reactions of Diverse Heteroarenes via π-System Activation. Organic letters, 2014, 16, 3208-3211 |
1516517 | CIF | C15 H15 N O2 | P 1 21/n 1 | 10.2481; 10.1664; 12.1731 90; 93.195; 90 | 1266.3 | Zhang, Zhi-Jing; Quan, Xue-Jing; Ren, Zhi-Hui; Wang, Yao-Yu; Guan, Zheng-Hui A Facile BPO-Mediated ortho-Hydroxylation and Benzoylation of N-Alkyl Anilines for Synthesis of 2-Benzamidophenols. Organic letters, 2014, 16, 3292-3295 |
1516518 | CIF | C14 H13 N O2 | P 1 21/c 1 | 8.226; 11.711; 13.239 90; 106.88; 90 | 1220.4 | Zhang, Zhi-Jing; Quan, Xue-Jing; Ren, Zhi-Hui; Wang, Yao-Yu; Guan, Zheng-Hui A Facile BPO-Mediated ortho-Hydroxylation and Benzoylation of N-Alkyl Anilines for Synthesis of 2-Benzamidophenols. Organic letters, 2014, 16, 3292-3295 |
1516522 | CIF | C26 H31 N O5 | P 21 21 21 | 7.495; 10.4454; 35.197 90; 90; 90 | 2755.5 | Letort, Aurélien; Aouzal, Rémi; Ma, Cong; Long, De-Liang; Prunet, Joëlle Highly efficient synthesis of the tricyclic core of taxol by cascade metathesis. Organic letters, 2014, 16, 3300-3303 |
1516523 | CIF | C15 H18 N2 O2 | P 1 21 1 | 6.546; 12.058; 8.846 90; 97.94; 90 | 691.5 | Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko Electroreductive Coupling of Optically Active α,β-Unsaturated Carbonyl Compounds with Diaryl Ketones: Asymmetric Synthesis of 4,5,5-Trisubstituted γ-Butyrolactones. Organic letters, 2014, 16, 3348-3351 |
1516524 | CIF | C24 H20 O2 | P 21 21 21 | 8.9315; 9.1942; 21.867 90; 90; 90 | 1795.7 | Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko Electroreductive Coupling of Optically Active α,β-Unsaturated Carbonyl Compounds with Diaryl Ketones: Asymmetric Synthesis of 4,5,5-Trisubstituted γ-Butyrolactones. Organic letters, 2014, 16, 3348-3351 |
1516525 | CIF | C35 H34 N2 O3 | P 21 21 21 | 8.284; 13.944; 23.978 90; 90; 90 | 2770 | Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko Electroreductive Coupling of Optically Active α,β-Unsaturated Carbonyl Compounds with Diaryl Ketones: Asymmetric Synthesis of 4,5,5-Trisubstituted γ-Butyrolactones. Organic letters, 2014, 16, 3348-3351 |
1516526 | CIF | C28 H30 N2 O3 | P 1 | 6.63; 8.27; 22.07 89.6; 87.7; 80 | 1191 | Kise, Naoki; Hamada, Yusuke; Sakurai, Toshihiko Electroreductive Coupling of Optically Active α,β-Unsaturated Carbonyl Compounds with Diaryl Ketones: Asymmetric Synthesis of 4,5,5-Trisubstituted γ-Butyrolactones. Organic letters, 2014, 16, 3348-3351 |
1516527 | CIF | C19 H22 N2 O4 | P 1 21/c 1 | 7.297; 12.192; 19.971 90; 94.898; 90 | 1770.2 | Patel, Pitambar; Chang, Sukbok N-substituted hydroxylamines as synthetically versatile amino sources in the iridium-catalyzed mild C-h amidation reaction. Organic letters, 2014, 16, 3328-3331 |
1516528 | CIF | C26 H29 F3 Ir N O4 | P 1 21/n 1 | 16.479; 8.855; 17.7803 90; 103.143; 90 | 2526.6 | Patel, Pitambar; Chang, Sukbok N-substituted hydroxylamines as synthetically versatile amino sources in the iridium-catalyzed mild C-h amidation reaction. Organic letters, 2014, 16, 3328-3331 |
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