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DOI number:10.1021/ol402687t
Journal:Organic Letters
Abstract:A mild procedure for C-7-selective CH alkenylation of various indolines under oxidative palladium(II) catalysis is reported. A fully substituted urea, formed by carbamoylation of the indoline nitrogen atom, functions as a directing group. Both R,β-unsaturated acceptors and styrenes participate in this direct CH functionalization. With a free NH group at the urea terminus, the nitrogen atom subsequently cyclizes in a 1,4-fashion to yield a six-membered ring.
Indexed by:Journal paper
Discipline:Natural Science
First-Level Discipline:Chemistry
Document Type:J
Volume:15
Page Number:5374–5377
Translation or Not:no
Included Journals:SCI、EI、SSCI
First Author:Lin-Yu Jiao
Professor
Supervisor of Doctorate Candidates
Supervisor of Master's Candidates
Name (English):Linyu Jiao
Name (Pinyin):jiaolinyu
E-Mail:
School/Department:School of Chemical Engineering
Administrative Position:Professor
Education Level:With Certificate of Graduation for Doctorate Study
Business Address:Room 517, School of Chemical Engineering
Gender:Male
Contact Information:+86-(0)15029011564
Degree:Doctoral degree
Status:Employed
Alma Mater:Technical University of Berlin
Discipline:Other specialties in Chemical Engineering and Technology
Chemical Engineering
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Honors and Titles:
仲英青年学者 2020-01-03
国家建设高水平大学公派研究生奖学金 2011-05-10
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