Crystallography Open Database

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Searching year of publication is 2018

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1548431 CIFC40 H50 B2 N2 O4P -18.4242; 15.698; 28.081
89.956; 87.717; 89.896
3710.6Katsuma, 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
1548432 CIFC49 H59 B2 N3 O4P -110.951; 14.21; 16.118
104.201; 92.6541; 111.94
2228.7Katsuma, 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
1548433 CIFC54 H69 B2 N3 O2P 1 21/c 110.6242; 20.635; 22.708
90; 100.578; 90
4893.7Katsuma, 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
1548434 CIFC37 H47 B2 N3 O2P 1 21/n 110.981; 10.43; 28.55
90; 94.578; 90
3259.5Katsuma, 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
1548435 CIFC37 H47 B2 N3 O2P 1 21/a 115.319; 13.7912; 17.481
90; 112.051; 90
3423Katsuma, 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 CIFC38 H48 B2 N2 O2P 1 21/n 18.565; 33.036; 11.991
90; 90.444; 90
3393Katsuma, 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 CIFC48 H56 B2 F3 N3 O2P 1 21/n 114.692; 11.21; 27.115
90; 105.567; 90
4302Katsuma, 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 CIFC45 H62 B2 N2 O4P -111.4491; 12.8149; 15.929
74.652; 86.76; 65.452
2046.2Katsuma, 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 CIFC49 H59 B2 N3 O4P -18.034; 10.856; 26.173
97.069; 97.132; 102.212
2187.4Katsuma, 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 CIFC53 H63 B2 N3 O2P -111.821; 12.93; 16.755
101.05; 95.8819; 111.862
2289.8Katsuma, 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 CIFC39 H37 B2 F3 N2 O2P 21 21 2116.004; 21.403; 32.93
90; 90; 90
11280Katsuma, 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 CIFC39 H47 B2 F3 N2 O2P 1 21/c 114.252; 17.527; 14.877
90; 93.855; 90
3707.8Katsuma, 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 CIFC89 H112 B4 N4 O4P -19.894; 12.714; 16.323
101.384; 91.511; 100.757
1973.3Katsuma, 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 CIFC38 H47 B2 Cl N2 O2P 1 21/c 110.777; 8.468; 38.298
90; 95.088; 90
3481Katsuma, 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 CIFC45 H64 B2 N2 O3P n a 2119.208; 13.253; 16.091
90; 90; 90
4096.2Katsuma, 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 CIFC22 H25 N O4P 21 21 2110.3192; 11.0867; 17.4057
90; 90; 90
1991.31Carter, 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 CIFC20 H23 N O2P 21 21 216.1094; 14.2823; 19.8409
90; 90; 90
1731.24Carter, 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 CIFC27 H21 N O2P -17.9717; 9.2791; 14.2492
95.3798; 105.336; 98.2795
996.24Carter, 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 CIFC23 H27 N O4P 1 21 19.495; 8.8357; 12.0617
90; 90.258; 90
1011.91Carter, 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 CIFC106 H66 B4 F40 O2 P2P n a 2123.2043; 30.9754; 14.803
90; 90; 90
10639.8Wang, 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 CIFC88 H62 B4 F40 O2 P2P -111.163; 16.2067; 24.8378
76.432; 87.505; 76.034
4238.6Wang, 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 CIFC31 H32 B F10 PP 1 21/n 117.6792; 8.532; 19.5972
90; 99.052; 90
2919.2Wang, 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 CIFC40 H34 B F10 PP 1 21/n 113.2212; 16.1944; 19.5088
90; 94.223; 90
4165.7Wang, 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 CIFC34 H38 B F10 PP -113.2091; 14.4202; 17.4143
102.465; 96.491; 91.561
3213.5Wang, 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
1548464 CIFC141 H111 B6 F60 O3 P3P 1 21/n 112.2916; 38.2278; 34.996
90; 90.268; 90
16443.8Wang, 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
1548465 CIFC144 H72 Mn3 N12 O70 Zr12I m -3 m38.4015; 38.4015; 38.4015
90; 90; 90
56630Gallagher, Audrey T.; Lee, Jung Yoon; Kathiresan, Venkatesan; Anderson, John S.; Hoffman, Brian M.; Harris, T. David
A structurally-characterized peroxomanganese(iv) porphyrin from reversible O<sub>2</sub> binding within a metal-organic framework.
Chemical science, 2018, 9, 1596-1603
1548466 CIFC144 H72 Mn3 N12 O52 Zr12I m -3 m38.672; 38.672; 38.672
90; 90; 90
57835Gallagher, Audrey T.; Lee, Jung Yoon; Kathiresan, Venkatesan; Anderson, John S.; Hoffman, Brian M.; Harris, T. David
A structurally-characterized peroxomanganese(iv) porphyrin from reversible O<sub>2</sub> binding within a metal-organic framework.
Chemical science, 2018, 9, 1596-1603
1548488 CIFC14 H30 Cl4 N4 Ni O4P c a 2112.5175; 13.082; 13.0989
90; 90; 90
2145Craig, Gavin A.; Sarkar, Arup; Woodall, Christopher H.; Hay, Moya A.; Marriott, Katie E. R.; Kamenev, Konstantin V.; Moggach, Stephen A.; Brechin, Euan K.; Parsons, Simon; Rajaraman, Gopalan; Murrie, Mark
Probing the origin of the giant magnetic anisotropy in trigonal bipyramidal Ni(ii) under high pressure.
Chemical science, 2018, 9, 1551-1559
1548489 CIFC14 H30 Cl4 N4 Ni O4P c a 2111.9968; 12.5527; 12.8642
90; 90; 90
1937.2Craig, Gavin A.; Sarkar, Arup; Woodall, Christopher H.; Hay, Moya A.; Marriott, Katie E. R.; Kamenev, Konstantin V.; Moggach, Stephen A.; Brechin, Euan K.; Parsons, Simon; Rajaraman, Gopalan; Murrie, Mark
Probing the origin of the giant magnetic anisotropy in trigonal bipyramidal Ni(ii) under high pressure.
Chemical science, 2018, 9, 1551-1559
1548490 CIFC14 H30 Cl4 N4 Ni O4P c a 2111.9924; 12.5546; 12.8611
90; 90; 90
1936.4Craig, Gavin A.; Sarkar, Arup; Woodall, Christopher H.; Hay, Moya A.; Marriott, Katie E. R.; Kamenev, Konstantin V.; Moggach, Stephen A.; Brechin, Euan K.; Parsons, Simon; Rajaraman, Gopalan; Murrie, Mark
Probing the origin of the giant magnetic anisotropy in trigonal bipyramidal Ni(ii) under high pressure.
Chemical science, 2018, 9, 1551-1559
1548491 CIFC14 H30 Cl4 N4 Ni O4P c a 2112.3181; 12.8429; 13.038
90; 90; 90
2062.61Craig, Gavin A.; Sarkar, Arup; Woodall, Christopher H.; Hay, Moya A.; Marriott, Katie E. R.; Kamenev, Konstantin V.; Moggach, Stephen A.; Brechin, Euan K.; Parsons, Simon; Rajaraman, Gopalan; Murrie, Mark
Probing the origin of the giant magnetic anisotropy in trigonal bipyramidal Ni(ii) under high pressure.
Chemical science, 2018, 9, 1551-1559
1548492 CIFC14 H30 Cl4 N4 Ni O4P c a 2112.2089; 12.7469; 12.9686
90; 90; 90
2018.2Craig, Gavin A.; Sarkar, Arup; Woodall, Christopher H.; Hay, Moya A.; Marriott, Katie E. R.; Kamenev, Konstantin V.; Moggach, Stephen A.; Brechin, Euan K.; Parsons, Simon; Rajaraman, Gopalan; Murrie, Mark
Probing the origin of the giant magnetic anisotropy in trigonal bipyramidal Ni(ii) under high pressure.
Chemical science, 2018, 9, 1551-1559
1548493 CIFC3 H4 Br Cl0 O2 PbP 41 21 29.0035; 9.0035; 14.39
90; 90; 90
1166.5Peng, Chengdong; Zhuang, Zewen; Yang, Huimin; Zhang, Guiyang; Fei, Honghan
Ultrastable, cationic three-dimensional lead bromide frameworks that intrinsically emit broadband white-light.
Chemical science, 2018, 9, 1627-1633
1548494 CIFC4 H4 Br4 O4 Pb3P b c n8.2193; 14.718; 10.7344
90; 90; 90
1298.56Peng, Chengdong; Zhuang, Zewen; Yang, Huimin; Zhang, Guiyang; Fei, Honghan
Ultrastable, cationic three-dimensional lead bromide frameworks that intrinsically emit broadband white-light.
Chemical science, 2018, 9, 1627-1633
1548495 CIFC3 H4 Br O2 PbP 41 21 28.9917; 8.9917; 14.354
90; 90; 90
1160.5Peng, Chengdong; Zhuang, Zewen; Yang, Huimin; Zhang, Guiyang; Fei, Honghan
Ultrastable, cationic three-dimensional lead bromide frameworks that intrinsically emit broadband white-light.
Chemical science, 2018, 9, 1627-1633
1548531 CIFC19 H46 Cl4 Eu N8 O ZnP b c a16.9858; 18.4496; 18.8816
90; 90; 90
5917.1Jenks, Tyler C.; Bailey, Matthew D.; Hovey, Jessica L.; Fernando, Shanilke; Basnayake, Gihan; Cross, Michael E.; Li, Wen; Allen, Matthew J.
First use of a divalent lanthanide for visible-light-promoted photoredox catalysis.
Chemical science, 2018, 9, 1273-1278
1548532 CIFC15 H12 N2C 1 2/c 122.851; 5.7145; 16.97
90; 98.174; 90
2193.5Joost, Maximilian; Transue, Wesley J.; Cummins, Christopher C.
Diazomethane umpolung atop anthracene: an electrophilic methylene transfer reagent.
Chemical science, 2018, 9, 1540-1543
1548533 CIFC27 H41 O2 W0.5P 21 21 215.0937; 17.6924; 9.6626
90; 90; 90
2580.3Joost, Maximilian; Transue, Wesley J.; Cummins, Christopher C.
Diazomethane umpolung atop anthracene: an electrophilic methylene transfer reagent.
Chemical science, 2018, 9, 1540-1543
1548534 CIFC68 H87 O4 P WP -113.4644; 13.7709; 18.7517
106.468; 110.976; 96.554
3021.7Joost, Maximilian; Transue, Wesley J.; Cummins, Christopher C.
Diazomethane umpolung atop anthracene: an electrophilic methylene transfer reagent.
Chemical science, 2018, 9, 1540-1543
1548543 CIFC14 H18 N2 O4P -16.746; 7.246; 7.434
77.801; 83.65; 88.409
353Zeng, Qingying; Mukherjee, Arijit; Müller, Peter; Rogers, Robin D.; Myerson, Allan S.
Exploring the role of ionic liquids to tune the polymorphic outcome of organic compounds.
Chemical science, 2018, 9, 1510-1520
1548544 CIFC24 H31 Al N2P -17.0719; 11.897; 15.148
76.92; 86.12; 85.2
1235.5Yu, Chao; Zhang, Pengfei; Gao, Fei; Zhang, Shaowen; Li, Xiaofang
A displacement-type fluorescent probe reveals active species in the coordinative polymerization of olefins
Polymer Chemistry, 2018, 9, 603
1548545 CIFC30 H43 Al N2P 1 21/n 18.6985; 11.354; 28.622
90; 94.73; 90
2817.2Yu, Chao; Zhang, Pengfei; Gao, Fei; Zhang, Shaowen; Li, Xiaofang
A displacement-type fluorescent probe reveals active species in the coordinative polymerization of olefins
Polymer Chemistry, 2018, 9, 603
1548546 CIFC48 H61 N4 Sc SiP 1 21/c 115.263; 11.695; 25.821
90; 106.57; 90
4417.7Yu, Chao; Zhang, Pengfei; Gao, Fei; Zhang, Shaowen; Li, Xiaofang
A displacement-type fluorescent probe reveals active species in the coordinative polymerization of olefins
Polymer Chemistry, 2018, 9, 603
1548547 CIFC26 H35 Al N2P 1 21/c 17.8769; 28.84; 10.921
90; 106.63; 90
2377.2Yu, Chao; Zhang, Pengfei; Gao, Fei; Zhang, Shaowen; Li, Xiaofang
A displacement-type fluorescent probe reveals active species in the coordinative polymerization of olefins
Polymer Chemistry, 2018, 9, 603
1548552 CIFEu F Mn PP 4/n m m :14.02916; 4.02916; 8.9505
90; 90; 90
145.304I.V. Plokhikh; D.O. Charkin; V.Yu. Verchenko; A.N. Kuznetsov; A.A. Tsirlin; S.M. Kazakov; A.V. Shevelkov
Synthesis, crystal structure and physical properties of europium - manganese fluoride pnictides, EuMnPnF (Pn = P, As, Sb)
Journal of Solid State Chemistry, 2018, 258, 682-690
1548553 CIFAs Eu F MnP 4/n m m :14.12265; 4.12265; 9.08462
90; 90; 90
154.404I.V. Plokhikh; D.O. Charkin; V.Yu. Verchenko; A.N. Kuznetsov; A.A. Tsirlin; S.M. Kazakov; A.V. Shevelkov
Synthesis, crystal structure and physical properties of europium - manganese fluoride pnictides, EuMnPnF (Pn = P, As, Sb)
Journal of Solid State Chemistry, 2018, 258, 682-690
1548554 CIFEu F Mn SbP 4/n m m :14.31203; 4.31203; 9.43557
90; 90; 90
175.441I.V. Plokhikh; D.O. Charkin; V.Yu. Verchenko; A.N. Kuznetsov; A.A. Tsirlin; S.M. Kazakov; A.V. Shevelkov
Synthesis, crystal structure and physical properties of europium - manganese fluoride pnictides, EuMnPnF (Pn = P, As, Sb)
Journal of Solid State Chemistry, 2018, 258, 682-690
1548564 CIFC17 H12 OP 1 21/c 120.011; 8.957; 13.2256
90; 92.118; 90
2368.9Xu, Wei; Fu, Yanyan; Liu, Huan; He, Qingguo; Cao, Huimin; Cheng, Jiangong
Attogram "Meth" Detection Enabled by Selective Organic Crystal Disaggregation via Directed Crystal Level Interactions.
Analytical chemistry, 2018, 90, 1402-1407
1548565 CIFC37 H51.88 Br4 Co N3 O ZnP 21 21 2112.6608; 17.559; 18.5345
90; 90; 90
4120.4Werth, Jacob; Uyeda, Christopher
Regioselective Simmons-Smith-type cyclopropanations of polyalkenes enabled by transition metal catalysis.
Chemical science, 2018, 9, 1604-1609
1548566 CIFC19 H14 B F6 N OP -19.0343; 10.2063; 11.0348
66.3381; 70.1856; 78.1262
873.89Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548567 CIFC27 H26 B Cl2 N O2P 1 21/n 114.1158; 8.9604; 18.8756
90; 90.0788; 90
2387.44Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548568 CIFC29 H24 B F6 N O2P -110.014; 11.7859; 23.0748
103.818; 98.0649; 96.9376
2584.47Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548569 CIFC18 H6 B3 F9 O3C 1 2/c 112.8358; 12.6583; 12.8851
90; 119.06; 90
1830Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548570 CIFC28 H22 B2 I2 O5P -110.635; 11.4814; 12.2457
83.1389; 87.0947; 64.1817
1336.36Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548571 CIFC29 H28 B Cl2 N O2P -19.2006; 11.4729; 13.1121
101.57; 99.773; 98.085
1314.22Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548572 CIFC26 H18 B F6 N O2P 1 21/n 110.1019; 11.7656; 19.567
90; 103.69; 90
2259.56Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548573 CIFC14.5 H13 B Cl1.5 D0.5 F6 N2 OP 1 c 111.75; 11.0269; 13.1973
90; 97.3307; 90
1695.95Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548574 CIFC25 H15 B3 F9 N O3P -110.372; 11.1795; 12.3123
106.545; 111.492; 96.8493
1232.74Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548575 CIFC18 H6 B3 F9 O3P b c n17.083; 13.093; 7.99
90; 90; 90
1787.1Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548576 CIFC46 H51 B3 N4 O3P 1 21/c 121.212; 11.2705; 18.8494
90; 114.886; 90
4087.9Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548577 CIFC28 H22 B2 Cl2 O5P -110.4296; 11.147; 11.7996
84.748; 87.958; 67.5356
1262.39Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548578 CIFC32 H33 B3 N2 O3P -111.2396; 15.2054; 17.9361
89.7333; 72.0196; 84.3291
2900.27Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548579 CIFC18 H6 B3 F9 O3C 1 2/c 112.8086; 12.6262; 12.8625
90; 119.598; 90
1808.74Arkhipenko, Sergey; Sabatini, Marco T.; Batsanov, Andrei S.; Karaluka, Valerija; Sheppard, Tom D.; Rzepa, Henry S.; Whiting, Andrew
Mechanistic insights into boron-catalysed direct amidation reactions.
Chemical science, 2018, 9, 1058-1072
1548586 CIFC25 H17 Au Cl F4 N2 O PP 1 21/n 119.942; 10.9697; 24.135
90; 112.7; 90
4870.7Arif, T.; Cazorla, C.; Bogliotti, N.; Saleh, N.; Blanchard, F.; Gandon, V.; Métivier, R.; Xie, J.; Voituriez, A.; Marinetti, A.
Bimetallic gold(i) complexes of photoswitchable phosphines: synthesis and uses in cooperative catalysis
Catalysis Science & Technology, 2018, 8, 710
1548587 CIFC25 H17 Au Cl F4 N2 O PP 1 21/n 116.0034; 8.3754; 19.2521
90; 111.188; 90
2406.01Arif, T.; Cazorla, C.; Bogliotti, N.; Saleh, N.; Blanchard, F.; Gandon, V.; Métivier, R.; Xie, J.; Voituriez, A.; Marinetti, A.
Bimetallic gold(i) complexes of photoswitchable phosphines: synthesis and uses in cooperative catalysis
Catalysis Science & Technology, 2018, 8, 710
1548588 CIFC37.85 H26.29 Au2 Cl7.11 F4 N2 P2P -111.051; 15.816; 16.857
109.459; 103.933; 104.747
2509.4Arif, T.; Cazorla, C.; Bogliotti, N.; Saleh, N.; Blanchard, F.; Gandon, V.; Métivier, R.; Xie, J.; Voituriez, A.; Marinetti, A.
Bimetallic gold(i) complexes of photoswitchable phosphines: synthesis and uses in cooperative catalysis
Catalysis Science & Technology, 2018, 8, 710
1548589 CIFC36.8 H24.8 Au2 Cl4.4 F4 N2 P2P 1 21/c 118.453; 18.5065; 11.1568
90; 97.085; 90
3781Arif, T.; Cazorla, C.; Bogliotti, N.; Saleh, N.; Blanchard, F.; Gandon, V.; Métivier, R.; Xie, J.; Voituriez, A.; Marinetti, A.
Bimetallic gold(i) complexes of photoswitchable phosphines: synthesis and uses in cooperative catalysis
Catalysis Science & Technology, 2018, 8, 710
1548590 CIFC39 H42 B N OC 1 2/c 138.4003; 9.7146; 18.3058
90; 114.338; 90
6222Shi, Yong-Gang; Wang, Jun-Wei; Li, Haijun; Hu, Guo-Fei; Li, Xue; Mellerup, Soren K.; Wang, Nan; Peng, Tai; Wang, Suning
A simple multi-responsive system based on aldehyde functionalized amino-boranes.
Chemical science, 2018, 9, 1902-1911
1548591 CIFC25 H27 B OP -18.488; 10.8609; 12.4693
97.707; 98.593; 105.796
1075.07Shi, Yong-Gang; Wang, Jun-Wei; Li, Haijun; Hu, Guo-Fei; Li, Xue; Mellerup, Soren K.; Wang, Nan; Peng, Tai; Wang, Suning
A simple multi-responsive system based on aldehyde functionalized amino-boranes.
Chemical science, 2018, 9, 1902-1911
1548592 CIFC27 H32 B N OP 1 21/n 112.3452; 9.0371; 20.4924
90; 91.199; 90
2285.7Shi, Yong-Gang; Wang, Jun-Wei; Li, Haijun; Hu, Guo-Fei; Li, Xue; Mellerup, Soren K.; Wang, Nan; Peng, Tai; Wang, Suning
A simple multi-responsive system based on aldehyde functionalized amino-boranes.
Chemical science, 2018, 9, 1902-1911
1548593 CIFC28 H34 B N OP 1 21/c 110.146; 16.684; 16.55
90; 103.602; 90
2722.9Shi, Yong-Gang; Wang, Jun-Wei; Li, Haijun; Hu, Guo-Fei; Li, Xue; Mellerup, Soren K.; Wang, Nan; Peng, Tai; Wang, Suning
A simple multi-responsive system based on aldehyde functionalized amino-boranes.
Chemical science, 2018, 9, 1902-1911
1548594 CIFC23 H37 B N2 Se2P 1 21/c 117.551; 15.552; 17.729
90; 93.183; 90
4832Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548595 CIFC49 H70 B2 N4 SP 1 21/c 118.966; 13.037; 18.816
90; 97.143; 90
4616.3Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548596 CIFC50 H78 B2 N4 O2 Se3C 1 2/c 116.059; 17.563; 17.928
90; 103.042; 90
4926.1Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548597 CIFC50 H78 B2 N4 O2 S3C 1 2/c 115.945; 17.53; 17.924
90; 102.905; 90
4883.5Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548598 CIFC37 H49 B N2 O Se2P 1 21/n 110.784; 16.852; 19.026
90; 91.03; 90
3457Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548599 CIFC48 H68 B2 N4 S2P -18.8508; 8.8654; 14.6186
75.639; 86.11; 80.401
1095.24Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548600 CIFC42 H62 B2 N4 SeP b c a17.8352; 16.7797; 28.365
90; 90; 90
8488.8Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548601 CIFC54 H86 B2 N4 O3 S4P b c a16.39; 17.61; 38.28
90; 90; 90
11049Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548602 CIFC37 H49 B N2 O S2P 1 21/n 110.672; 16.818; 18.902
90; 91.75; 90
3391Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548603 CIFC24 H34 B N2 SeP -18.8289; 8.8405; 14.667
85.939; 75.916; 79.987
1093Auerhammer, Dominic; Arrowsmith, Merle; Dewhurst, Rian D.; Kupfer, Thomas; Böhnke, Julian; Braunschweig, Holger
Closely related yet different: a borylene and its dimer are non-interconvertible but connected through reactivity.
Chemical science, 2018, 9, 2252-2260
1548613 CIFC17 H14 Br N OP 21 21 216.1624; 7.7041; 30.136
90; 90; 90
1430.7Luo, Hongwen; Yang, Zheng; Lin, Weilong; Zheng, Yangguangyan; Ma, Shengming
A catalytic highly enantioselective allene approach to oxazolines.
Chemical science, 2018, 9, 1964-1969
1548614 CIFC33 H37.5 B I2 N OP 1 21/n 113.751; 16.557; 28.155
90; 93.121; 90
6401Qi, Yanyu; Xu, Wenjun; Kang, Rui; Ding, Nannan; Wang, Yelei; He, Gang; Fang, Yu
Discrimination of saturated alkanes and relevant volatile compounds <i>via</i> the utilization of a conceptual fluorescent sensor array based on organoboron-containing polymers.
Chemical science, 2018, 9, 1892-1901
1548615 CIFC35.5 H61 Li Ni O8.25P -111.4664; 24.2697; 28.3765
67.455; 88.576; 85.754
7273.2Iwasaki, Takanori; Fukuoka, Asuka; Yokoyama, Wataru; Min, Xin; Hisaki, Ichiro; Yang, Tao; Ehara, Masahiro; Kuniyasu, Hitoshi; Kambe, Nobuaki
Nickel-catalyzed coupling reaction of alkyl halides with aryl Grignard reagents in the presence of 1,3-butadiene: mechanistic studies of four-component coupling and competing cross-coupling reactions.
Chemical science, 2018, 9, 2195-2211
1548616 CIFC15 H21 Ga O6P n a 2115.7074; 32.8408; 13.412
90; 90; 90
6918.5Li, Wenzhe; Zhang, Cuiling; Ma, Yunping; Liu, Chong; Fan, Jiandong; Mai, Yaohua; Schropp, Ruud E. I.
In situ induced core/shell stabilized hybrid perovskites via gallium(iii) acetylacetonate intermediate towards highly efficient and stable solar cells
Energy & Environmental Science, 2018, 11, 286
1548617 CIFC16 H28 Ga I N O6P 1 21/n 112.3537; 12.2717; 15.5166
90; 112.273; 90
2176.82Li, Wenzhe; Zhang, Cuiling; Ma, Yunping; Liu, Chong; Fan, Jiandong; Mai, Yaohua; Schropp, Ruud E. I.
In situ induced core/shell stabilized hybrid perovskites via gallium(iii) acetylacetonate intermediate towards highly efficient and stable solar cells
Energy & Environmental Science, 2018, 11, 286
1548632 CIFC27 H14 In N O8F d d d13.706; 34.19; 45.37
90; 90; 90
21261Hou, Sheng-Li; Dong, Jie; Jiang, Xiao-Lei; Jiao, Zhuo-Hao; Wang, Chu-Ming; Zhao, Bin
Interpenetration-Depended Luminescent Probe in Indium-Organic Frameworks for Selectively Detecting Nitrofurazone in Water.
Analytical chemistry, 2018
1548633 CIFC35 H35 In N4 O10P -19.8441; 13.3787; 13.8506
112.559; 97.112; 91.975
1664.9Hou, Sheng-Li; Dong, Jie; Jiang, Xiao-Lei; Jiao, Zhuo-Hao; Wang, Chu-Ming; Zhao, Bin
Interpenetration-Depended Luminescent Probe in Indium-Organic Frameworks for Selectively Detecting Nitrofurazone in Water.
Analytical chemistry, 2018
1548634 CIFC19 H27 N O SP b c a13.4779; 8.1983; 31.894
90; 90; 90
3524.2Shen, Xianwang; Gong, Honghong; Zhou, Yang; Zhao, Yucheng; Lin, Jun; Chen, Mao
Unsymmetrical difunctionalization of cyclooctadiene under continuous flow conditions: expanding the scope of ring opening metathesis polymerization.
Chemical science, 2018, 9, 1846-1853
1548635 CIFC23 H24 O2P 21 21 219.7798; 10.6568; 17.5257
90; 90; 90
1826.55Zheng, Xinxin; Guo, Rui; Zhang, Guozhu; Zhang, Dayong
Rhodium(i)-catalyzed asymmetric [4 + 2] cycloaddition reactions of 2-alkylenecyclobutanols with cyclic enones through C-C bond cleavage: efficient access to <i>trans</i>-bicyclic compounds.
Chemical science, 2018, 9, 1873-1877
1548636 CIFC8 H14 Ag N O4P 21 21 217.786; 8.024; 16.081
90; 90; 90
1004.7Fang, Yinzhi; Zhang, Han; Huang, Zhen; Scinto, Samuel L.; Yang, Jeffrey C.; Am Ende, Christopher W.; Dmitrenko, Olga; Johnson, Douglas S.; Fox, Joseph M.
Photochemical syntheses, transformations, and bioorthogonal chemistry of <i>trans</i>-cycloheptene and sila <i>trans</i>-cycloheptene Ag(i) complexes.
Chemical science, 2018, 9, 1953-1963
1548637 CIFC18 H20 Ag N O3 SiP 1 21/c 116.509; 8.4282; 13.9655
90; 114.69; 90
1765.53Fang, Yinzhi; Zhang, Han; Huang, Zhen; Scinto, Samuel L.; Yang, Jeffrey C.; Am Ende, Christopher W.; Dmitrenko, Olga; Johnson, Douglas S.; Fox, Joseph M.
Photochemical syntheses, transformations, and bioorthogonal chemistry of <i>trans</i>-cycloheptene and sila <i>trans</i>-cycloheptene Ag(i) complexes.
Chemical science, 2018, 9, 1953-1963
1548638 CIFC30.71 H44.57 Br1.14 Fe N2 O2.86I 1 a 115.186; 13.4178; 17.1643
90; 112.449; 90
3232.4Fleischauer, Valerie E.; Muñoz Iii, Salvador B; Neate, Peter G. N.; Brennessel, William W.; Neidig, Michael L.
NHC and nucleophile chelation effects on reactive iron(ii) species in alkyl-alkyl cross-coupling.
Chemical science, 2018, 9, 1878-1891
1548639 CIFC39 H60 Fe N2 O4P -110.0953; 10.9483; 17.657
88.7501; 75.1691; 88.9205
1885.9Fleischauer, Valerie E.; Muñoz Iii, Salvador B; Neate, Peter G. N.; Brennessel, William W.; Neidig, Michael L.
NHC and nucleophile chelation effects on reactive iron(ii) species in alkyl-alkyl cross-coupling.
Chemical science, 2018, 9, 1878-1891
1548640 CIFC33 H46 Fe N2 O4C 1 c 111.2603; 22.9235; 16.1864
90; 103.878; 90
4056.2Fleischauer, Valerie E.; Muñoz Iii, Salvador B; Neate, Peter G. N.; Brennessel, William W.; Neidig, Michael L.
NHC and nucleophile chelation effects on reactive iron(ii) species in alkyl-alkyl cross-coupling.
Chemical science, 2018, 9, 1878-1891
1548649 CIFC45 H58 N4 O7P 21 21 2111.9273; 15.9773; 20.8434
90; 90; 90
3972.04Zhang, Yu; Yuan, Yu-Xi; Goto, Masuo; Guo, Ling-Li; Li, Xiao-Nian; Morris-Natschke, Susan L.; Lee, Kuo-Hsiung; Hao, Xiao-Jiang
Taburnaemines A‒I, Cytotoxic Vobasinyl-Iboga-Type Bisindole Alkaloids from Tabernaemontana corymbosa
Journal of Natural Products, 2018
1548650 CIFC47 H56 N4 O8P 21 21 219.4439; 18.2011; 24.5795
90; 90; 90
4224.95Zhang, Yu; Yuan, Yu-Xi; Goto, Masuo; Guo, Ling-Li; Li, Xiao-Nian; Morris-Natschke, Susan L.; Lee, Kuo-Hsiung; Hao, Xiao-Jiang
Taburnaemines A‒I, Cytotoxic Vobasinyl-Iboga-Type Bisindole Alkaloids from Tabernaemontana corymbosa
Journal of Natural Products, 2018
1548651 CIFC250.5 H168.5 B5 Co6 F41 N47 O21.25 S7P -121.2508; 21.6182; 39.5929
93.208; 101.624; 118.521
15407.3Rizzuto, Felix J.; Kieffer, Marion; Nitschke, Jonathan R.
Quantified structural speciation in self-sorted CoII6L<sub>4</sub> cage systems.
Chemical science, 2018, 9, 1925-1930
1548652 CIFC273 H263.5 B60.5 Co6 F19.5 N62.5 O20.5 S6.5P -125.0303; 26.7592; 34.5514
68.113; 88.8092; 66.5154
19472.1Rizzuto, Felix J.; Kieffer, Marion; Nitschke, Jonathan R.
Quantified structural speciation in self-sorted CoII6L<sub>4</sub> cage systems.
Chemical science, 2018, 9, 1925-1930
1548653 CIFC92 H130 Cl2 N4 Ni2 O5P 1 21/n 115.5829; 39.582; 16.2027
90; 110.448; 90
9364.1Clarke, Ryan M.; Jeen, Tiffany; Rigo, Serena; Thompson, John R.; Kaake, Loren G.; Thomas, Fabrice; Storr, Tim
Exploiting exciton coupling of ligand radical intervalence charge transfer transitions to tune NIR absorption.
Chemical science, 2018, 9, 1610-1620

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