Crystallography Open Database

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Searching journal of publication like 'Organic letters' volume of publication is 15

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1512080 CIFC55 H58 Cl4 N4 O2 PdP -111.3639; 13.2788; 18.587
75.262; 79.729; 70.965
2550.2Kuriyama, Masami; Matsuo, Seira; Shinozawa, Mina; Onomura, Osamu
Ether-imidazolium carbenes for suzuki-miyaura cross-coupling of heteroaryl chlorides with aryl/heteroarylboron reagents.
Organic letters, 2013, 15, 2716-2719
1512081 CIFC48 H60 Cl2 N4 O2 PdP -19.525; 9.705; 13.059
69.341; 87.28; 87.5
1127.8Kuriyama, Masami; Matsuo, Seira; Shinozawa, Mina; Onomura, Osamu
Ether-imidazolium carbenes for suzuki-miyaura cross-coupling of heteroaryl chlorides with aryl/heteroarylboron reagents.
Organic letters, 2013, 15, 2716-2719
1512082 CIFC30 H33 Cl N2 O PdP 1 21/c 19.363; 14.332; 19.941
90; 98.871; 90
2643.9Kuriyama, Masami; Matsuo, Seira; Shinozawa, Mina; Onomura, Osamu
Ether-imidazolium carbenes for suzuki-miyaura cross-coupling of heteroaryl chlorides with aryl/heteroarylboron reagents.
Organic letters, 2013, 15, 2716-2719
1512083 CIFC48 H60 F12 N4 O4 Pd Sb2C 1 c 111.9986; 23.347; 19.104
90; 92.8783; 90
5344.9Kuriyama, Masami; Matsuo, Seira; Shinozawa, Mina; Onomura, Osamu
Ether-imidazolium carbenes for suzuki-miyaura cross-coupling of heteroaryl chlorides with aryl/heteroarylboron reagents.
Organic letters, 2013, 15, 2716-2719
1512084 CIFC39 H34 N2 O2 SP 1 21/n 113.2199; 11.4301; 21.0851
90; 90.191; 90
3186Xing, Yanpeng; Zhao, Hongyang; Shang, Qiongyi; Wang, Jing; Lu, Ping; Wang, Yanguang
Parallel Copper Catalysis: Diastereoselective Synthesis of Polyfunctionalized Azetidin-2-imines.
Organic letters, 2013, 15, 2668-2671
1512085 CIFC37 H30 N2 O2 SP -111.6466; 11.9984; 12.9367
67.388; 64.731; 85.073
1502.5Xing, Yanpeng; Zhao, Hongyang; Shang, Qiongyi; Wang, Jing; Lu, Ping; Wang, Yanguang
Parallel Copper Catalysis: Diastereoselective Synthesis of Polyfunctionalized Azetidin-2-imines.
Organic letters, 2013, 15, 2668-2671
1512086 CIFC25 H22 Cl N3 O5P -110.8394; 11.4488; 11.4719
74.667; 81.908; 63.495
1228.2Feng, Xian; Wang, Qian; Lin, Wei; Dou, Guo-Lan; Huang, Zhi-Bin; Shi, Da-Qing
Highly Efficient Synthesis of Polysubstituted Pyrroles via Four-Component Domino Reaction
Organic Letters, 2013, 15, 2542
1512087 CIFC13 H20 O3P 21 21 216.0852; 11.7873; 35.4794
90; 90; 90
2544.87Alam, Rauful; Raducan, Mihai,; Eriksson, Lars; Szabó, Kálmán J.
Selective Formation of Adjacent Stereocenters by Allylboration of Ketones under Mild Neutral Conditions
Organic Letters, 2013, 15, 2546
1512088 CIFC18 H16 Br N OP 1 21/c 18.3171; 11.418; 17.1359
90; 97.692; 90
1612.66Alam, Rauful; Raducan, Mihai,; Eriksson, Lars; Szabó, Kálmán J.
Selective Formation of Adjacent Stereocenters by Allylboration of Ketones under Mild Neutral Conditions
Organic Letters, 2013, 15, 2546
1512089 CIFC19 H16 Br N O2C 1 2/c 128.7975; 7.8077; 16.5405
90; 110.356; 90
3486.7Alam, Rauful; Raducan, Mihai,; Eriksson, Lars; Szabó, Kálmán J.
Selective Formation of Adjacent Stereocenters by Allylboration of Ketones under Mild Neutral Conditions
Organic Letters, 2013, 15, 2546
1512090 CIFC28 H37 N O5 SiP 1 21 17.5725; 15.488; 11.7937
90; 100.558; 90
1359.78Wales, Steven M.; Walker, Morgan M.; Johnson, Jeffrey S.
Asymmetric Synthesis of Indole Homo-Michael Adducts via Dynamic Kinetic Friedel‒Crafts Alkylation with Cyclopropanes
Organic Letters, 2013, 15, 2558
1512091 CIFC28 H29 N O5P 1 21/c 19.528; 9.517; 25.51
90; 94.72; 90
2305Kise, Naoki; Sueyoshi, Akinori; Takeuchi, Shin-Ichirou; Sakurai, Toshihiko
Electroreductive intermolecular coupling of 3-methoxycarbonylindoles with ketones.
Organic letters, 2013, 15, 2746-2749
1512092 CIFC16 H21 N O3P 1 21/c 110.696; 15.927; 17.75
90; 91.808; 90
3022.3Kise, Naoki; Sueyoshi, Akinori; Takeuchi, Shin-Ichirou; Sakurai, Toshihiko
Electroreductive intermolecular coupling of 3-methoxycarbonylindoles with ketones.
Organic letters, 2013, 15, 2746-2749
1512093 CIFC112 H62 N4 Ni0.5 O5 SP 1 21/c 117.1633; 14.5957; 31.045
90; 103.967; 90
7547.2Futagoishi, Tsukasa; Murata, Michihisa; Wakamiya, Atsushi; Sasamori, Takahiro; Murata, Yasujiro
Expansion of Orifices of Open C60 Derivatives and Formation of an Open C59S Derivative by Reaction with Sulfur.
Organic letters, 2013, 15, 2750-2753
1512094 CIFC112 H61.04 N4.96 Ni0.5 O4.52 S2P 1 21/c 117.122; 14.8245; 31.17
90; 102.629; 90
7720.3Futagoishi, Tsukasa; Murata, Michihisa; Wakamiya, Atsushi; Sasamori, Takahiro; Murata, Yasujiro
Expansion of Orifices of Open C60 Derivatives and Formation of an Open C59S Derivative by Reaction with Sulfur.
Organic letters, 2013, 15, 2750-2753
1512095 CIFC88 H36 N2 O3.75 S2P 1 21/c 118.8292; 15.7485; 20.6189
90; 116.272; 90
5482.58Futagoishi, Tsukasa; Murata, Michihisa; Wakamiya, Atsushi; Sasamori, Takahiro; Murata, Yasujiro
Expansion of Orifices of Open C60 Derivatives and Formation of an Open C59S Derivative by Reaction with Sulfur.
Organic letters, 2013, 15, 2750-2753
1512096 CIFC16 H10 Cl N3 O3P -17.2229; 13.4298; 15.5038
95.483; 98.449; 99.913
1454.06Liang, Lei; Wang, Wei; Xu, Fengrong; Niu, Yan; Sun, Qi; Xu, Ping
Relay Catalysis by a Multifunctional Cu Catalyst in a Tandem Dehydro-/Dehalogenation Sequence along with N-Arylation.
Organic letters, 2013, 15, 2770-2773
1512097 CIFC19 H19 N O2 SP -19.1257; 9.1641; 10.7395
101.582; 92.848; 103.302
851.9Zhu, Can; Ma, Shengming
Coupling and Cyclization of o-Iodoanilines and Propargylic Bromides via Allenes: An Efficient Entry to Indomethacin.
Organic letters, 2013, 15, 2782-2785
1512098 CIFC25 H20 N2 O2P -18.843; 13.5211; 18.1943
111.348; 99.037; 93.744
1983.2Lin, Chi-Hui; Yang, Ding-Yah
Synthesis of coumarin/pyrrole-fused heterocycles and their photochemical and redox-switching properties.
Organic letters, 2013, 15, 2802-2805
1512099 CIFC20 H18 N2 O2P -18.6766; 13.6112; 14.5535
99.558; 106.757; 91.782
1617.2Lin, Chi-Hui; Yang, Ding-Yah
Synthesis of coumarin/pyrrole-fused heterocycles and their photochemical and redox-switching properties.
Organic letters, 2013, 15, 2802-2805

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