Para-Selective Dehydrogenative Phenothiazination of Hydroquinolines and Indolines
Author(s) -
Pooja Y. Vemuri,
Yongchao Wang,
Frédéric W. Patureau
Publication year - 2019
Publication title -
organic letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.94
H-Index - 239
eISSN - 1523-7060
pISSN - 1523-7052
DOI - 10.1021/acs.orglett.9b03729
Subject(s) - chemistry , combinatorial chemistry , stereochemistry , medicinal chemistry
Nitrogen-containing heterocyclic systems, such as hydroquinolines, indolines, and phenothiazines, are prevalent in pharmaceuticals, natural products, and organic materials. It is therefore important to develop novel reaction strategies that give access to such biologically relevant scaffolds. This report demonstrates a novel robust, para -selective C-N bond formation between phenothiazines and quinolines or indolines under extremely mild and user-friendly conditions. Furthermore, we bring forward a surprising discovery arising from the homocoupling of indolines through an unprecedented C5-H functionalization.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom