| Literature DB >> 29154551 |
Takahide Fukuyama1, Tomohiro Nishikawa1, Keiichi Yamada1, Davide Ravelli2, Maurizio Fagnoni2, Ilhyong Ryu1,3.
Abstract
Tetrabutylammonium decatungstate (TBADT)-photocatalyzed C-H functionalization of alkylpyridines was investigated. Unlike alkylbenzene counterparts, alkylation of α-C-H bonds did not proceed for the reaction of 2- and 4-alkylpyridines and reluctantly proceeded for 3-alkylpyridines, which allow site-selective C(sp3)-H functionalization at nonbenzylic positions. The observed nonbenzylic site selectivities are rationalized by the polar inductive effects of pyridyl groups in the SH2 transition states. Consecutive γ-functionalization and α-bromofunctionalization were successfully carried out in selected cases.Entities:
Year: 2017 PMID: 29154551 DOI: 10.1021/acs.orglett.7b03339
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005