Crystallography Open Database
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Searching journal of publication like 'The Journal of organic chemistry' volume of publication is 79
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 4029375 | CIF | C17 H14 Cl N O3 | P 21 21 21 | 7.1652; 12.6049; 16.4098 90; 90; 90 | 1482.08 | Wu, Xiang; Li, Ming-Li; Chen, Dian-Feng; Chen, Shu-Sen Enantioselective construction of [6,5,6]-carbocyclic systems by organo/metal-catalyzed sequential reactions. The Journal of organic chemistry, 2014, 79, 4743-4750 |
| 4029376 | CIF | C13 H17 N O2 | P c a 21 | 19.234; 5.6695; 10.7313 90; 90; 90 | 1170.2 | Shimizu, Tomoaki; Koya, Shunsuke; Yamasaki, Ryu; Mutoh, Yuichiro; Azumaya, Isao; Katagiri, Kosuke; Saito, Shinichi Acid-Mediated Ring-Expansion Reaction of N-Aryl-2-vinylazetidines: Synthesis and Unanticipated Reactivity of Tetrahydrobenzazocines. The Journal of organic chemistry, 2014, 79, 4367-4377 |
| 4029377 | CIF | C13 H17 N O2 | P 1 21/c 1 | 11.401; 12; 8.479 90; 92.305; 90 | 1159.1 | Shimizu, Tomoaki; Koya, Shunsuke; Yamasaki, Ryu; Mutoh, Yuichiro; Azumaya, Isao; Katagiri, Kosuke; Saito, Shinichi Acid-Mediated Ring-Expansion Reaction of N-Aryl-2-vinylazetidines: Synthesis and Unanticipated Reactivity of Tetrahydrobenzazocines. The Journal of organic chemistry, 2014, 79, 4367-4377 |
| 4029378 | CIF | C27 H19 N O2 | P -1 | 5.7246; 10.9332; 16.289 77.753; 86.78; 80.766 | 983.1 | Wang, Meining; Zhang, Chi; Sun, Li-Ping; Ding, Chunyong; Zhang, Ao Naphthoquinone-directed C-h annulation and csp(3)-h bond cleavage: one-pot synthesis of tetracyclic naphthoxazoles. The Journal of organic chemistry, 2014, 79, 4553-4560 |
| 4029379 | CIF | C38 H40 Br2 Cl4 N4 O4 | P 1 21/c 1 | 12.7758; 12.4749; 24.7006 90; 96.782; 90 | 3909.2 | DeBlase, Catherine R.; Finke, Ryan T.; Porras, Jonathan A.; Tanski, Joseph M.; Nadeau, Jocelyn M. C-Shaped Diastereomers Containing Cofacial Thiophene-Substituted Quinoxaline Rings: Synthesis, Photophysical Properties, and X-ray Crystallography. The Journal of organic chemistry, 2014, 79, 4312-4321 |
| 4029380 | CIF | C42 H36 Cl8 N4 O4 S2 | P -1 | 10.5303; 11.5381; 18.5812 86.903; 74.816; 77.042 | 2123.3 | DeBlase, Catherine R.; Finke, Ryan T.; Porras, Jonathan A.; Tanski, Joseph M.; Nadeau, Jocelyn M. C-Shaped Diastereomers Containing Cofacial Thiophene-Substituted Quinoxaline Rings: Synthesis, Photophysical Properties, and X-ray Crystallography. The Journal of organic chemistry, 2014, 79, 4312-4321 |
| 4029381 | CIF | C41 H33 Cl7 N4 O4 S2 | P 1 21/n 1 | 11.149; 32.7727; 11.5886 90; 98.527; 90 | 4187.5 | DeBlase, Catherine R.; Finke, Ryan T.; Porras, Jonathan A.; Tanski, Joseph M.; Nadeau, Jocelyn M. C-Shaped Diastereomers Containing Cofacial Thiophene-Substituted Quinoxaline Rings: Synthesis, Photophysical Properties, and X-ray Crystallography. The Journal of organic chemistry, 2014, 79, 4312-4321 |
| 4029382 | CIF | C34 H26 O | P -1 | 9.14; 11.564; 11.837 81.82; 89.37; 73.3 | 1185.6 | Guo, Biao; Zheng, Liyao; Yang, Lichen; Hua, Ruimao Synthesis of Chrysene Derivatives via Copper-Catalyzed One-Pot Dimerization of 2-Alkynyl-1-acetylbenzenes. The Journal of organic chemistry, 2014, 79, 4352-4357 |
| 4029383 | CIF | C23 H21 N O | P -1 | 5.6805; 10.0159; 15.1868 91.566; 97.711; 96.58 | 849.8 | Chen, Jian-Ming; Chang, Chin-Jung; Ke, Yao-Jin; Liu, Rai-Shung Catalytic Formal [4 + 2] Cycloadditions between Unactivated Allenes and N-Hydroxyaniline Catalyzed by AuCl3/CuCl2/O2. The Journal of organic chemistry, 2014, 79, 4306-4311 |
| 4029384 | CIF | C34 H38 N2 O | I 1 2/a 1 | 45.341; 6.3267; 19.1637 90; 94.165; 90 | 5482.8 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029385 | CIF | C33 H34 Cl2 O5 | P -1 | 9.3084; 11.0123; 14.2584 96.174; 92.581; 96.04 | 1442.7 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029386 | CIF | C34 H32 F6 N2 O | C 1 2/c 1 | 34.0554; 9.9336; 23.0128 90; 129.512; 90 | 6006.1 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029387 | CIF | C32 H30 O4 | P 1 21/n 1 | 9.568; 9.0894; 28.1687 90; 95.888; 90 | 2436.83 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029388 | CIF | C36 H38 O8 | C 1 2/c 1 | 27.2623; 7.994; 18.8173 90; 130.377; 90 | 3124.1 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029389 | CIF | C32 H24 F6 O2 | P 1 21/c 1 | 16.1001; 19.841; 17.6455 90; 115.919; 90 | 5069.7 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029390 | CIF | C34 H38 N2 O3 | P b c a | 21.8256; 10.1693; 25.5637 90; 90; 90 | 5673.9 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029391 | CIF | C34 H34 O6 | P -1 | 9.148; 12.84; 13.415 107.886; 101.844; 92.212 | 1458.9 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029392 | CIF | C32 H26 Br2 O4 | P -1 | 9.8125; 11.0615; 13.6335 70.815; 78.876; 81.967 | 1366.69 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029393 | CIF | C38 H44 O3 | P 1 21/c 1 | 25.956; 6.182; 19.745 90; 90.35; 90 | 3168 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029394 | CIF | C34 H34 O4 | P 1 21/n 1 | 15.8962; 23.9751; 15.4845 90; 115.677; 90 | 5318.6 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029395 | CIF | C36 H38 O8 | P c c n | 14.3696; 24.357; 8.882 90; 90; 90 | 3108.7 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029396 | CIF | C30 H26 | P 1 21/c 1 | 11.2069; 11.0239; 18.5291 90; 90.694; 90 | 2288.99 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029397 | CIF | C35 H40 Cl2 N2 O3 | P 1 21/c 1 | 13.809; 10.376; 21.761 90; 94.95; 90 | 3106.3 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029398 | CIF | C32 H32 O5 | P 1 21/c 1 | 18.9058; 9.7027; 16.0143 90; 114.597; 90 | 2671.05 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029399 | CIF | C34 H34 | P -1 | 12.3177; 14.2234; 16.6636 84.729; 73.553; 66.674 | 2570.47 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029400 | CIF | C32 H26 F6 O3 | P 1 21/c 1 | 10.7473; 24.594; 10.5723 90; 107.995; 90 | 2657.8 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029401 | CIF | C36 H38 O8 | P -1 | 10.0529; 12.8185; 13.4817 102.978; 111.583; 93.167 | 1555.9 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029402 | CIF | C30 H26 F2 O3 | P b c a | 20.42; 10.0168; 23.6874 90; 90; 90 | 4845.1 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029403 | CIF | C32 H26 F6 O3 | P 1 21/n 1 | 8.7765; 26.7134; 23.5585 90; 90; 90 | 5523.3 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029404 | CIF | C32 H30 O4 | P n a 21 | 14.6805; 15.8549; 10.8348 90; 90; 90 | 2521.88 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029405 | CIF | C32 H30 O4 | P -1 | 10.2734; 15.6266; 16.2315 107.797; 90.011; 91.077 | 2480.59 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029406 | CIF | C32 H32 O5 | C 1 2/c 1 | 24.0553; 9.1097; 24.6742 90; 98.351; 90 | 5349.7 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029407 | CIF | C34 H34 O6 | P -1 | 10.3767; 12.3787; 21.9131 87.931; 84.966; 88.166 | 2800.88 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029408 | CIF | C34.5 H37 N O1.5 | P 1 n 1 | 10.9755; 11.2553; 22.7841 90; 94.201; 90 | 2807.02 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029409 | CIF | C30 H24 N2 O6 | C 1 2/c 1 | 21.8582; 11.2916; 20.2879 90; 99.753; 90 | 4935 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029410 | CIF | C32 H24 N2 O2 | P 1 21/c 1 | 9.5203; 23.024; 11.6499 90; 100.456; 90 | 2511.2 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029411 | CIF | C36 H38 O8 | P -1 | 6.867; 14.544; 15.106 83.765; 89.255; 89.174 | 1499.5 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029412 | CIF | C32 H32 O5 | P -1 | 8.0506; 13.1393; 13.3586 68.499; 76.048; 76.844 | 1260.68 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029413 | CIF | C34 H38 O6 | P 1 21/n 1 | 12.0322; 11.9498; 20.361 90; 100.039; 90 | 2882.73 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029414 | CIF | C34 H32 F6 N2 O | P 1 2/c 1 | 23.741; 8.7785; 28.77 90; 103.418; 90 | 5832.3 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029415 | CIF | C32 H30 | P 1 21/c 1 | 10.3391; 22.1229; 10.9627 90; 110.352; 90 | 2350.97 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029416 | CIF | C34 H34 O6 | P 1 21/c 1 | 11.834; 21.682; 21.523 90; 94.25; 90 | 5507 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029417 | CIF | C32 H31 N O | P 1 21/c 1 | 11.173; 25.204; 9.16 90; 102.144; 90 | 2522 | Hong, Fong-Jiao; Low, Yun-Yee; Chong, Kam-Weng; Thomas, Noel F.; Kam, Toh-Seok Biomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathways. The Journal of organic chemistry, 2014, 79, 4528-4543 |
| 4029418 | CIF | C33 H33 Cl2 N3 O3 | P 1 21 1 | 11.7883; 17.9576; 14.1225 90; 90.594; 90 | 2989.4 | Tan, Wei; Du, Bai-Xiang; Li, Xin; Zhu, Xu; Shi, Feng; Tu, Shu-Jiang Catalytic Asymmetric Aza-ene Reaction of 3-Indolylmethanols with Cyclic Enaminones: Enantioselective Approach to C3-Functionalized Indoles. The Journal of organic chemistry, 2014, 79, 4635-4643 |
| 4029419 | CIF | C31 H28 Cl N3 O2 | P 32 2 1 | 14.5913; 14.5913; 24.0429 90; 90; 120 | 4433.1 | Tan, Wei; Du, Bai-Xiang; Li, Xin; Zhu, Xu; Shi, Feng; Tu, Shu-Jiang Catalytic Asymmetric Aza-ene Reaction of 3-Indolylmethanols with Cyclic Enaminones: Enantioselective Approach to C3-Functionalized Indoles. The Journal of organic chemistry, 2014, 79, 4635-4643 |
| 4029420 | CIF | C14 H12 O2 | P 1 21/n 1 | 6.644; 10.4808; 15.2251 90; 100.429; 90 | 1042.68 | Thangaraj, Manikandan; Bhojgude, Sachin Suresh; Bisht, Rajesh H.; Gonnade, Rajesh G.; Biju, Akkattu T. Diels-Alder Reaction of Tropones with Arynes: Synthesis of Functionalized Benzobicyclo[3.2.2]nonatrienones. The Journal of organic chemistry, 2014, 79, 4757-4762 |
| 4029425 | CIF | C20 H29 I N O11 | P 1 21 1 | 9.1343; 6.8955; 20.2243 90; 91.191; 90 | 1273.56 | Islam, Maidul; Tirukoti, Nishanth D.; Nandi, Shyamapada; Hotha, Srinivas Hypervalent iodine mediated synthesis of C-2 deoxy glycosides and amino Acid glycoconjugates. The Journal of organic chemistry, 2014, 79, 4470-4476 |
| 4029426 | CIF | C20 H20 N2 O3 | P 1 21/c 1 | 10.12; 10.669; 16.642 90; 106.45; 90 | 1723.3 | En, Da; Zou, Gong-Feng; Guo, Yuan; Liao, Wei-Wei Nucleophilic Phosphine-Catalyzed Intramolecular Michael Reactions of N-Allylic Substituted α-Amino Nitriles: Construction of Functionalized Pyrrolidine Rings via 5-endo-trig Cyclizations. The Journal of organic chemistry, 2014, 79, 4456-4462 |
| 4029427 | CIF | C66 H132 Cl6 N12 O39 | P 1 21 1 | 13.685; 20.3904; 17.52 90; 105.773; 90 | 4704.7 | Faggi, Enrico; Moure, Alejandra; Bolte, Michael; Vicent, Cristian; Luis, Santiago V.; Alfonso, Ignacio Pseudopeptidic cages as receptors for N-protected dipeptides. The Journal of organic chemistry, 2014, 79, 4590-4601 |
| 4029428 | CIF | C25 H25 Br N4 O4 | C 1 2 1 | 41.527; 11.0922; 26.113 90; 123.323; 90 | 10051 | Li, Tian-Ze; Wang, Xi-Bo; Sha, Feng; Wu, Xin-Yan Organocatalyzed enantioselective mannich reaction of pyrazoleamides with isatin-derived ketimines. The Journal of organic chemistry, 2014, 79, 4332-4339 |
| 4029429 | CIF | C27 H20 N2 Se | P 1 21/c 1 | 13.77; 9.3234; 17.015 90; 101.934; 90 | 2137.2 | Murai, Toshiaki; Yamaguchi, Kirara; Hori, Fumihiko; Maruyama, Toshifumi Reaction of selenoamide dianions with thio- and selenoformamides leading to the formation of 5-aminoselenazoles: photophysical and electrochemical properties. The Journal of organic chemistry, 2014, 79, 4930-4939 |
| 4029430 | CIF | C18 H18 N2 | P -1 | 9.0667; 9.4296; 9.8594 112.774; 98.136; 107.001 | 711.6 | Orejarena Pacheco, Julio Cesar; Opatz, Till Ring Expansion of 1,2,3,4-Tetrahydroisoquinolines to Dibenzo[c,f]azonines. An Unexpected [1,4]-Sigmatropic Rearrangement of Nitrile-Stabilized Ammonium Ylides. The Journal of organic chemistry, 2014, 79, 5182-5192 |
| 4029431 | CIF | C20 H22 N2 O2 | P 1 21/c 1 | 14.3891; 9.2391; 13.2215 90; 107.576; 90 | 1675.64 | Orejarena Pacheco, Julio Cesar; Opatz, Till Ring Expansion of 1,2,3,4-Tetrahydroisoquinolines to Dibenzo[c,f]azonines. An Unexpected [1,4]-Sigmatropic Rearrangement of Nitrile-Stabilized Ammonium Ylides. The Journal of organic chemistry, 2014, 79, 5182-5192 |
| 4029432 | CIF | C25 H29 N O6 | P 21 21 21 | 6.4802; 13.1979; 25.4488 90; 90; 90 | 2176.51 | Selfridge, Brandon R.; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C. Synthesis of Enantiopure 10-Nornaltrexones in the Search for Toll-like Receptor 4 Antagonists and Opioid Ligands. The Journal of organic chemistry, 2014, 79, 5007-5018 |
| 4029433 | CIF | C18 H21 N O3 | P 21 21 21 | 5.8822; 15.7145; 16.2267 90; 90; 90 | 1499.93 | Selfridge, Brandon R.; Deschamps, Jeffrey R.; Jacobson, Arthur E.; Rice, Kenner C. Synthesis of Enantiopure 10-Nornaltrexones in the Search for Toll-like Receptor 4 Antagonists and Opioid Ligands. The Journal of organic chemistry, 2014, 79, 5007-5018 |
| 4029434 | CIF | C27 H23 N3 O4 | P 1 21/n 1 | 9.4852; 16.6744; 15.2017 90; 94.942; 90 | 2395.36 | Cui, Bao-Dong; Zuo, Jian; Zhao, Jian-Qiang; Zhou, Ming-Qiang; Wu, Zhi-Jun; Zhang, Xiao-Mei; Yuan, Wei-Cheng Tandem Michael addition-ring transformation reactions of 3-hydroxyoxindoles/3-aminooxindoles with olefinic azlactones: direct access to structurally diverse spirocyclic oxindoles. The Journal of organic chemistry, 2014, 79, 5305-5314 |
| 4029435 | CIF | C23 H18 N2 O4 S | P 1 21/n 1 | 10.2604; 15.8897; 13.009 90; 108.475; 90 | 2011.61 | Cui, Bao-Dong; Zuo, Jian; Zhao, Jian-Qiang; Zhou, Ming-Qiang; Wu, Zhi-Jun; Zhang, Xiao-Mei; Yuan, Wei-Cheng Tandem Michael addition-ring transformation reactions of 3-hydroxyoxindoles/3-aminooxindoles with olefinic azlactones: direct access to structurally diverse spirocyclic oxindoles. The Journal of organic chemistry, 2014, 79, 5305-5314 |
| 4029436 | CIF | C32 H36 O8 | P 1 21/c 1 | 23.162; 11.5821; 11.2981 90; 100.997; 90 | 2975.2 | Vibhute, Amol M.; Sureshan, Kana M. Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding. The Journal of organic chemistry, 2014, 79, 4892-4908 |
| 4029437 | CIF | C25 H32 O7 | P 1 21/c 1 | 12.15; 10.181; 18.898 90; 95.579; 90 | 2326.6 | Vibhute, Amol M.; Sureshan, Kana M. Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding. The Journal of organic chemistry, 2014, 79, 4892-4908 |
| 4029438 | CIF | C36 H38 Cl2 O7 | P -1 | 12.0165; 16.3915; 18.4237 114.762; 103.433; 92.396 | 3165.08 | Vibhute, Amol M.; Sureshan, Kana M. Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding. The Journal of organic chemistry, 2014, 79, 4892-4908 |
| 4029439 | CIF | C28 H44 O8 | C 1 c 1 | 46.9596; 12.7191; 20.5382 90; 107.083; 90 | 11725.9 | Vibhute, Amol M.; Sureshan, Kana M. Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding. The Journal of organic chemistry, 2014, 79, 4892-4908 |
| 4029440 | CIF | C23 H36 O7 | P -1 | 17.077; 17.49; 17.638 102.333; 92.957; 117.285 | 4505.6 | Vibhute, Amol M.; Sureshan, Kana M. Strength from Weakness: Conformational Divergence between Solid and Solution States of Substituted Cyclitols Facilitated by CH···O Hydrogen Bonding. The Journal of organic chemistry, 2014, 79, 4892-4908 |
| 4029445 | CIF | C24 H18 O2 | P 21 21 21 | 6.993; 8.884; 26.801 90; 90; 90 | 1665 | Mori, Hiroki; Chen, Xi-Chao; Chang, Ning-Hui; Hamao, Shino; Kubozono, Yoshihiro; Nakajima, Kiyohiko; Nishihara, Yasushi Synthesis of methoxy-substituted picenes: substitution position effect on their electronic and single-crystal structures. The Journal of organic chemistry, 2014, 79, 4973-4983 |
| 4029446 | CIF | C24 H18 O2 | P 21 21 21 | 6.2114; 7.8271; 34.589 90; 90; 90 | 1681.6 | Mori, Hiroki; Chen, Xi-Chao; Chang, Ning-Hui; Hamao, Shino; Kubozono, Yoshihiro; Nakajima, Kiyohiko; Nishihara, Yasushi Synthesis of methoxy-substituted picenes: substitution position effect on their electronic and single-crystal structures. The Journal of organic chemistry, 2014, 79, 4973-4983 |
| 4029447 | CIF | C26 H22 O4 | P 1 21/n 1 | 7.043; 19.934; 13.754 90; 90.379; 90 | 1931 | Mori, Hiroki; Chen, Xi-Chao; Chang, Ning-Hui; Hamao, Shino; Kubozono, Yoshihiro; Nakajima, Kiyohiko; Nishihara, Yasushi Synthesis of methoxy-substituted picenes: substitution position effect on their electronic and single-crystal structures. The Journal of organic chemistry, 2014, 79, 4973-4983 |
| 4029448 | CIF | C18 H15 F3 N2 O2 S | P 1 21/n 1 | 12.393; 10.745; 13.09 90; 100.07; 90 | 1716.2 | Wang, Nuancheng; Li, Renhe; Li, Liubo; Xu, Shansheng; Song, Haibin; Wang, Baiquan Rhodium(III)-Catalyzed Intermolecular Amidation with Azides via C(sp(3))-H Functionalization. The Journal of organic chemistry, 2014, 79, 5379-5385 |
| 4029449 | CIF | C21 H25 N O3 | P 21 21 21 | 10.1714; 10.7715; 16.287 90; 90; 90 | 1784.4 | Curto, John M.; Kozlowski, Marisa C. α-Allyl-α-aryl α-Amino Esters in the Asymmetric Synthesis of Acyclic and Cyclic Amino Acid Derivatives by Alkene Metathesis. The Journal of organic chemistry, 2014, 79, 5359-5364 |
| 4029450 | CIF | C23 H28 F3 N O7 | P 21 21 21 | 8.9709; 14.6155; 18.1662 90; 90; 90 | 2381.8 | Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium. The Journal of organic chemistry, 2014, 79, 5287-5300 |
| 4029451 | CIF | C14 H23 N O5 | P 1 21 1 | 7.321; 11.808; 9.419 90; 110.277; 90 | 763.8 | Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium. The Journal of organic chemistry, 2014, 79, 5287-5300 |
| 4029452 | CIF | C24 H38 N2 O7 | P 21 21 2 | 16.598; 11.093; 13.208 90; 90; 90 | 2431.9 | Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium. The Journal of organic chemistry, 2014, 79, 5287-5300 |
| 4029453 | CIF | C24 H38 N2 O7 | P 21 21 2 | 11.046; 16.939; 13.237 90; 90; 90 | 2476.8 | Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium. The Journal of organic chemistry, 2014, 79, 5287-5300 |
| 4029454 | CIF | C25 H34 N2 O7 S | P 21 21 21 | 9.909; 12.774; 19.563 90; 90; 90 | 2476.2 | Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium. The Journal of organic chemistry, 2014, 79, 5287-5300 |
| 4029455 | CIF | C34 H48 Br N3 O10 | P 21 21 21 | 10.0129; 17.402; 20.03 90; 90; 90 | 3490.1 | Wang, Siyuan; Otani, Yuko; Liu, Xin; Kawahata, Masatoshi; Yamaguchi, Kentaro; Ohwada, Tomohiko Robust trans-Amide Helical Structure of Oligomers of Bicyclic Mimics of β-Proline: Impact of Positional Switching of Bridgehead Substituent on Amide cis-trans Equilibrium. The Journal of organic chemistry, 2014, 79, 5287-5300 |
| 4029456 | CIF | C19 H21 Cl N4 O | P 1 21/n 1 | 7.583; 8.075; 28.833 90; 95.49; 90 | 1757.4 | Martinez-Ariza, Guillermo; Ayaz, Muhammad; Medda, Federico; Hulme, Christopher Synthesis of diverse nitrogen-enriched heterocyclic scaffolds using a suite of tunable one-pot multicomponent reactions. The Journal of organic chemistry, 2014, 79, 5153-5162 |
| 4029457 | CIF | C18 H18 F N5 O3 | C 1 2/c 1 | 21.4045; 9.0833; 17.5993 90; 94.482; 90 | 3411.3 | Martinez-Ariza, Guillermo; Ayaz, Muhammad; Medda, Federico; Hulme, Christopher Synthesis of diverse nitrogen-enriched heterocyclic scaffolds using a suite of tunable one-pot multicomponent reactions. The Journal of organic chemistry, 2014, 79, 5153-5162 |
| 4029458 | CIF | C14 H15 Br Cl N3 O3 | P -1 | 8.9862; 9.873; 10.3897 115.309; 100.343; 104.653 | 761.34 | Martinez-Ariza, Guillermo; Ayaz, Muhammad; Medda, Federico; Hulme, Christopher Synthesis of diverse nitrogen-enriched heterocyclic scaffolds using a suite of tunable one-pot multicomponent reactions. The Journal of organic chemistry, 2014, 79, 5153-5162 |
| 4029459 | CIF | C18 H17 Cl O3 | P 21 21 21 | 4.878; 16.418; 19.847 90; 90; 90 | 1589.5 | Zeng, Zhongyi; Yang, Dingqiao; Long, Yuhua; Pan, Xuejing; Huang, Guobao; Zuo, Xiongjun; Zhou, Wen Nickel-catalyzed asymmetric ring opening of oxabenzonorbornadienes with arylboronic acids. The Journal of organic chemistry, 2014, 79, 5249-5257 |
| 4029460 | CIF | C12 H19 N O4 | P -1 | 11.119; 11.175; 18.547 77.91; 84.55; 60.74 | 1966 | Zhou, Lili; Yao, Yanmin; Xu, Wenbo; Liang, Guangxin Total Syntheses of (±)-Omphadiol and (±)-Pyxidatol C through a Cis-Fused 5,7-Carbocyclic Common Intermediate. The Journal of organic chemistry, 2014, 79, 5345-5350 |
| 4029461 | CIF | C14 H19 Cl2 O P | P 1 21 1 | 6.547; 14.435; 7.735 90; 108.659; 90 | 692.6 | Fokin, Andrey A.; Yurchenko, Raisa I.; Tkachenko, Boryslav A.; Fokina, Natalie A.; Gunawan, Maria A.; Poinsot, Didier; Dahl, Jeremy E. P.; Carlson, Robert M. K.; Serafin, Michael; Cattey, Hélène; Hierso, Jean-Cyrille; Schreiner, Peter R. Selective preparation of diamondoid phosphonates. The Journal of organic chemistry, 2014, 79, 5369-5373 |
| 4029462 | CIF | C26 H31 Cl2 O P | P 1 21/m 1 | 8.5927; 12.5125; 9.8811 90; 107.977; 90 | 1010.5 | Fokin, Andrey A.; Yurchenko, Raisa I.; Tkachenko, Boryslav A.; Fokina, Natalie A.; Gunawan, Maria A.; Poinsot, Didier; Dahl, Jeremy E. P.; Carlson, Robert M. K.; Serafin, Michael; Cattey, Hélène; Hierso, Jean-Cyrille; Schreiner, Peter R. Selective preparation of diamondoid phosphonates. The Journal of organic chemistry, 2014, 79, 5369-5373 |
| 4029463 | CIF | C22 H27 Cl2 O P | P 1 21/n 1 | 13.7657; 6.5028; 20.58 90; 91.615; 90 | 1841.5 | Fokin, Andrey A.; Yurchenko, Raisa I.; Tkachenko, Boryslav A.; Fokina, Natalie A.; Gunawan, Maria A.; Poinsot, Didier; Dahl, Jeremy E. P.; Carlson, Robert M. K.; Serafin, Michael; Cattey, Hélène; Hierso, Jean-Cyrille; Schreiner, Peter R. Selective preparation of diamondoid phosphonates. The Journal of organic chemistry, 2014, 79, 5369-5373 |
| 4029464 | CIF | C18 H26 N2 O5 S Si | P 1 21 1 | 7.1772; 7.3897; 20.5531 90; 91.23; 90 | 1089.83 | Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions. The Journal of organic chemistry, 2014, 79, 5121-5133 |
| 4029465 | CIF | C17 H20 N2 O5 S | P 21 21 21 | 6.1282; 8.0712; 36.366 90; 90; 90 | 1798.7 | Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions. The Journal of organic chemistry, 2014, 79, 5121-5133 |
| 4029466 | CIF | C19 H28 N2 O5 S Si | P 1 21 1 | 7.2155; 7.3686; 21.8244 90; 91.207; 90 | 1160.11 | Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions. The Journal of organic chemistry, 2014, 79, 5121-5133 |
| 4029467 | CIF | C11 H15 N O2 S | P 1 21/n 1 | 12.4009; 7.2781; 12.4672 90; 94.562; 90 | 1121.66 | Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions. The Journal of organic chemistry, 2014, 79, 5121-5133 |
| 4029468 | CIF | C22 H31 Co2 N O9 S Si | P 21 21 21 | 12.5959; 12.7985; 18.2292 90; 90; 90 | 2938.7 | Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions. The Journal of organic chemistry, 2014, 79, 5121-5133 |
| 4029469 | CIF | C12 H12 N2 O4 S | P 1 21 1 | 7.7299; 8.0026; 21.4995 90; 91.981; 90 | 1329.15 | Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions. The Journal of organic chemistry, 2014, 79, 5121-5133 |
| 4029470 | CIF | C16 H16 N2 O4 S | P 1 21 1 | 7.6048; 7.3949; 13.9958 90; 94.525; 90 | 784.62 | Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions. The Journal of organic chemistry, 2014, 79, 5121-5133 |
| 4029471 | CIF | C11 H14 N2 O4 S | P 1 21 1 | 7.3131; 12.6022; 28.2003 90; 95.198; 90 | 2588.28 | Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions. The Journal of organic chemistry, 2014, 79, 5121-5133 |
| 4029472 | CIF | C19 H28 N2 O5 S Si | P 1 21 1 | 9.956; 7.927; 14.0034 90; 96.822; 90 | 1097.34 | Kelley, Brandon T.; Carroll, Patrick; Joullié, Madeleine M Possible Reason for the Unusual Regioselectivity in Nucleophilic Ring Opening of Trisubstituted Aziridines under Mildly Basic Conditions. The Journal of organic chemistry, 2014, 79, 5121-5133 |
| 4029474 | CIF | C29 H26 N6 | P 1 21/n 1 | 9.5645; 15.6682; 17.0313 90; 95.23; 90 | 2541.7 | Jiang, Bo; Fan, Wei; Sun, Mu-Yan; Ye, Qin; Wang, Shu-Liang; Tu, Shu-Jiang; Li, Guigen Domino Reaction of Arylglyoxals with Pyrazol-5-amines: Selective Access to Pyrazolo-Fused 1,7-Naphthyridines, 1,3-Diazocanes, and Pyrroles. The Journal of organic chemistry, 2014, 79, 5258-5268 |
| 4029475 | CIF | C28 H22 Br2 N4 O | P 1 21/c 1 | 18.4011; 6.1969; 23.223 90; 105.394; 90 | 2553.1 | Jiang, Bo; Fan, Wei; Sun, Mu-Yan; Ye, Qin; Wang, Shu-Liang; Tu, Shu-Jiang; Li, Guigen Domino Reaction of Arylglyoxals with Pyrazol-5-amines: Selective Access to Pyrazolo-Fused 1,7-Naphthyridines, 1,3-Diazocanes, and Pyrroles. The Journal of organic chemistry, 2014, 79, 5258-5268 |
| 4029476 | CIF | C26 H20 Cl2 N6 | P 1 21/n 1 | 9.585; 12.7985; 18.4861 90; 91.299; 90 | 2267.2 | Jiang, Bo; Fan, Wei; Sun, Mu-Yan; Ye, Qin; Wang, Shu-Liang; Tu, Shu-Jiang; Li, Guigen Domino Reaction of Arylglyoxals with Pyrazol-5-amines: Selective Access to Pyrazolo-Fused 1,7-Naphthyridines, 1,3-Diazocanes, and Pyrroles. The Journal of organic chemistry, 2014, 79, 5258-5268 |
| 4029477 | CIF | C36 H30 N6 O2 | C 1 2/c 1 | 32.018; 9.2309; 21.6503 90; 110.711; 90 | 5985.3 | Jiang, Bo; Fan, Wei; Sun, Mu-Yan; Ye, Qin; Wang, Shu-Liang; Tu, Shu-Jiang; Li, Guigen Domino Reaction of Arylglyoxals with Pyrazol-5-amines: Selective Access to Pyrazolo-Fused 1,7-Naphthyridines, 1,3-Diazocanes, and Pyrroles. The Journal of organic chemistry, 2014, 79, 5258-5268 |
| 4029478 | CIF | C47 H55 Cl3 N8 O8 | C 1 2/c 1 | 47.727; 14.35; 17.94 90; 102.5; 90 | 11996 | Shang, Jie; Gallagher, Nolan M.; Bie, Fusheng; Li, Qiaolian; Che, Yanke; Wang, Ying; Jiang, Hua Aromatic triazole foldamers induced by C-h···x (x = f, cl) intramolecular hydrogen bonding. The Journal of organic chemistry, 2014, 79, 5134-5144 |
| 4029479 | CIF | C37 H37 F3 N6 O6 | P 1 21/c 1 | 9.6484; 13.075; 28.303 90; 98.2; 90 | 3534 | Shang, Jie; Gallagher, Nolan M.; Bie, Fusheng; Li, Qiaolian; Che, Yanke; Wang, Ying; Jiang, Hua Aromatic triazole foldamers induced by C-h···x (x = f, cl) intramolecular hydrogen bonding. The Journal of organic chemistry, 2014, 79, 5134-5144 |
| 4029480 | CIF | C55 H103 N18 O11 | P 1 21 1 | 10.379; 33.918; 19.627 90; 99.06; 90 | 6823 | Fremaux, Juliette; Kauffmann, Brice; Guichard, Gilles Synthesis and folding propensity of aliphatic oligoureas containing repeats of proline-type units. The Journal of organic chemistry, 2014, 79, 5494-5502 |
| 4029481 | CIF | C58 H111 N19 O11 | C 1 2 1 | 18.609; 20; 21.577 90; 107.06; 90 | 7677 | Fremaux, Juliette; Kauffmann, Brice; Guichard, Gilles Synthesis and folding propensity of aliphatic oligoureas containing repeats of proline-type units. The Journal of organic chemistry, 2014, 79, 5494-5502 |
| 4029482 | CIF | C20 H37 B2 N3 O5 | P 21 21 21 | 10.4871; 11.1272; 19.6809 90; 90; 90 | 2296.6 | Müller, Matthias; Maichle-Mössmer, Cäcilia; Bettinger, Holger F. Boryl azides in 1,3-dipolar cycloadditions. The Journal of organic chemistry, 2014, 79, 5478-5483 |
| 4029483 | CIF | C8 H15 N3 O | P 1 21/n 1 | 7.2695; 15.2273; 8.6831 90; 107.665; 90 | 915.9 | Müller, Matthias; Maichle-Mössmer, Cäcilia; Bettinger, Holger F. Boryl azides in 1,3-dipolar cycloadditions. The Journal of organic chemistry, 2014, 79, 5478-5483 |
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