Crystallography Open Database
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Result: there are 959 entries in the selection
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Searching journal of publication like 'Chemical science' volume of publication is 9
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1548435 | CIF | C37 H47 B2 N3 O2 | P 1 21/a 1 | 15.319; 13.7912; 17.481 90; 112.051; 90 | 3423 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548436 | CIF | C38 H48 B2 N2 O2 | P 1 21/n 1 | 8.565; 33.036; 11.991 90; 90.444; 90 | 3393 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548437 | CIF | C48 H56 B2 F3 N3 O2 | P 1 21/n 1 | 14.692; 11.21; 27.115 90; 105.567; 90 | 4302 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548438 | CIF | C45 H62 B2 N2 O4 | P -1 | 11.4491; 12.8149; 15.929 74.652; 86.76; 65.452 | 2046.2 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548439 | CIF | C49 H59 B2 N3 O4 | P -1 | 8.034; 10.856; 26.173 97.069; 97.132; 102.212 | 2187.4 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548440 | CIF | C53 H63 B2 N3 O2 | P -1 | 11.821; 12.93; 16.755 101.05; 95.8819; 111.862 | 2289.8 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548441 | CIF | C39 H37 B2 F3 N2 O2 | P 21 21 21 | 16.004; 21.403; 32.93 90; 90; 90 | 11280 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548442 | CIF | C39 H47 B2 F3 N2 O2 | P 1 21/c 1 | 14.252; 17.527; 14.877 90; 93.855; 90 | 3707.8 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548443 | CIF | C89 H112 B4 N4 O4 | P -1 | 9.894; 12.714; 16.323 101.384; 91.511; 100.757 | 1973.3 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548444 | CIF | C38 H47 B2 Cl N2 O2 | P 1 21/c 1 | 10.777; 8.468; 38.298 90; 95.088; 90 | 3481 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548445 | CIF | C45 H64 B2 N2 O3 | P n a 21 | 19.208; 13.253; 16.091 90; 90; 90 | 4096.2 | Katsuma, Yuhei; Asakawa, Hiroki; Yamashita, Makoto Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and <i>ortho</i>-functionalized pyridine derivatives. Chemical science, 2018, 9, 1301-1310 |
| 1548455 | CIF | C22 H25 N O4 | P 21 21 21 | 10.3192; 11.0867; 17.4057 90; 90; 90 | 1991.31 | Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench. Chemical science, 2018, 9, 1352-1357 |
| 1548456 | CIF | C20 H23 N O2 | P 21 21 21 | 6.1094; 14.2823; 19.8409 90; 90; 90 | 1731.24 | Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench. Chemical science, 2018, 9, 1352-1357 |
| 1548457 | CIF | C27 H21 N O2 | P -1 | 7.9717; 9.2791; 14.2492 95.3798; 105.336; 98.2795 | 996.24 | Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench. Chemical science, 2018, 9, 1352-1357 |
| 1548458 | CIF | C23 H27 N O4 | P 1 21 1 | 9.495; 8.8357; 12.0617 90; 90.258; 90 | 1011.91 | Carter, Nicholas; Li, Xiabing; Reavey, Lewis; Meijer, Anthony J. H. M.; Coldham, Iain Synthesis and kinetic resolution of substituted tetrahydroquinolines by lithiation then electrophilic quench. Chemical science, 2018, 9, 1352-1357 |
| 1548459 | CIF | C106 H66 B4 F40 O2 P2 | P n a 21 | 23.2043; 30.9754; 14.803 90; 90; 90 | 10639.8 | Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical science, 2018, 9, 1544-1550 |
| 1548460 | CIF | C88 H62 B4 F40 O2 P2 | P -1 | 11.163; 16.2067; 24.8378 76.432; 87.505; 76.034 | 4238.6 | Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical science, 2018, 9, 1544-1550 |
| 1548461 | CIF | C31 H32 B F10 P | P 1 21/n 1 | 17.6792; 8.532; 19.5972 90; 99.052; 90 | 2919.2 | Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical science, 2018, 9, 1544-1550 |
| 1548462 | CIF | C40 H34 B F10 P | P 1 21/n 1 | 13.2212; 16.1944; 19.5088 90; 94.223; 90 | 4165.7 | Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical science, 2018, 9, 1544-1550 |
| 1548463 | CIF | C34 H38 B F10 P | P -1 | 13.2091; 14.4202; 17.4143 102.465; 96.491; 91.561 | 3213.5 | Wang, Long; Dong, Shunxi; Daniliuc, Constantin G.; Liu, Lei; Grimme, Stefan; Knitsch, Robert; Eckert, Hellmut; Hansen, Michael Ryan; Kehr, Gerald; Erker, Gerhard Formation of macrocyclic ring systems by carbonylation of trifunctional P/B/B frustrated Lewis pairs. Chemical science, 2018, 9, 1544-1550 |
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