Enantioselective Synthesis of beta-Arylamines via Chiral Phosphoric Acid-Catalyzed Asymmetric Reductive Amination

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초록

A new method for the synthesis of chiral beta-aryl amines via chiral phosphoric acid-catalyzed enantioselective reductive amination of benzyl methyl ketone derivatives with Hantzsch ester was developed. Various chiral beta-aryl amines were obtained in high yields and with good to high enantioselectivities. This transformation is applicable to gram-scale reactions, and the catalyst loading can be reduced to 1 mol % without sacrificing any catalytic efficacy. Furthermore, the resulting beta-aryl amine was successfully converted into a tetrahydroisoquinoline compound without any loss of enantioselectivity.

키워드

TRANSFER HYDROGENATION; BRONSTED ACID; DERIVATIVES; KETONES; ACTIVATION; AMINES; TETRAHYDROISOQUINOLINES; BENZOTHIAZOLINE; SEQUENCE; IMINES
제목
Enantioselective Synthesis of beta-Arylamines via Chiral Phosphoric Acid-Catalyzed Asymmetric Reductive Amination
저자
Kim, Kyung-Hee; Lee, Chun-Young; Cheon, Cheol-Hong
DOI
10.1021/acs.joc.5b00812
발행일
2015-06-19
유형
Article
저널명
The Journal of Organic Chemistry
권
80
호
12
페이지
6367 ~ 6374