TY - JOUR
T1 - Palladium-catalyzed domino C-H/N-H functionalization
T2 - An efficient approach to nitrogen-bridged heteroacenes
AU - Kamimoto, Natsuyo
AU - Schollmeyer, Dieter
AU - Mitsudo, Koichi
AU - Suga, Seiji
AU - Waldvogel, Siegfried R.
N1 - Publisher Copyright:
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Copyright:
Copyright 2015 Elsevier B.V., All rights reserved.
PY - 2015/5/1
Y1 - 2015/5/1
N2 - Palladium-catalyzed domino C-H/N-H functionalization for the synthesis of novel nitrogen-bridged thienoacenes and 10H-benzo[4,5]thieno[3,2-b]indole derivatives from dihaloarene is reported. This domino sequence consists of initial C-H functionalization of the benzo[b]thiophene moiety, followed by Buchwald-Hartwig coupling. This transformation is also useful for the synthesis of highly π-extended compounds. Extended heteroacenes: A twofold arylation protocol for the efficient synthesis of 9H-benzo[4,5]thieno[3,2-b]thieno[3,4-d]pyrroles and 10H-benzo[4,5]thieno[3,2-b]indoles was developed (see scheme). The selectivity of this novel sequence allows the construction of highly π-extended heteroacenes.
AB - Palladium-catalyzed domino C-H/N-H functionalization for the synthesis of novel nitrogen-bridged thienoacenes and 10H-benzo[4,5]thieno[3,2-b]indole derivatives from dihaloarene is reported. This domino sequence consists of initial C-H functionalization of the benzo[b]thiophene moiety, followed by Buchwald-Hartwig coupling. This transformation is also useful for the synthesis of highly π-extended compounds. Extended heteroacenes: A twofold arylation protocol for the efficient synthesis of 9H-benzo[4,5]thieno[3,2-b]thieno[3,4-d]pyrroles and 10H-benzo[4,5]thieno[3,2-b]indoles was developed (see scheme). The selectivity of this novel sequence allows the construction of highly π-extended heteroacenes.
KW - C-H activation
KW - amination
KW - domino reactions
KW - heterocycles
KW - palladium
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U2 - 10.1002/chem.201500897
DO - 10.1002/chem.201500897
M3 - Article
AN - SCOPUS:84929340713
SN - 0947-6539
VL - 21
SP - 8257
EP - 8261
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 22
ER -