Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mai Nagase"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 391-397 (2020)
Hexa-peri-hexabenzocoronene (HBC) is known to be a poorly soluble polycyclic aromatic hydrocarbon for which direct functionalization methods have been very limited. Herein, the synthesis of hexaborylated HBC from unsubstituted HBC is described. Iridi
Externí odkaz:
https://doaj.org/article/43a19f3524354e7185e1f3c2b073aed0
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 80:994-999
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 391-397 (2020)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
Hexa-peri-hexabenzocoronene (HBC) is known to be a poorly soluble polycyclic aromatic hydrocarbon for which direct functionalization methods have been very limited. Herein, the synthesis of hexaborylated HBC from unsubstituted HBC is described. Iridi
Publikováno v:
Tetrahedron. 123:132907
Autor:
Kenichiro Itami, Lawrence T. Scott, M. Kuwayama, Mai Nagase, Kenta Kato, Hsing-An Lin, Yasutomo Segawa
Publikováno v:
Chemical Science. 10:9038-9041
The regioselective ten-fold borylation of warped nanographene (WNG: C80H30) was achieved by modifying the reaction conditions of a previously reported Ir-catalyzed C–H borylation, affording decaborylated WNG in high yield (75%) from pristine WNG. T