Affiliation:
1. Department of Chemistry, Shanghai University
2. State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Science
Abstract
AbstractHerein, a direct method for the synthesis of 3-fluoroindoles and 3,3-difluoroindolines from easily accessible 2,2-difluoro-2-phenylethan-1-amines is presented. This protocol was performed by Pd-catalyzed direct C–H/N–H coupling and employed picolinamide as a directing group. By controlling the temperature for this transformation, various 3,3-difluoroindolines and 3-fluoroindoles could be isolated with moderate to good yields.
Funder
Science and Technology Commission of Shanghai Municipality
State Key Laboratory of Drug Research
Subject
Organic Chemistry,Catalysis
Cited by
2 articles.
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