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Enantioselective Synthesis of beta-Arylamines via Chiral Phosphoric Acid-Catalyzed Asymmetric Reductive Amination
- Kim, Kyung-Hee;
- Lee, Chun-Young;
- Cheon, Cheol-Hong
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31초록
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
- 발행일
- 2015-06-19
- 유형
- Article
- 권
- 80
- 호
- 12
- 페이지
- 6367 ~ 6374
- 언어
- ENG
- 출판사
- AMER CHEMICAL SOC
- 발행국가
- 미국
- 분량
- 8 페이지
- ISSN
- E 1520-6904
P 0022-3263