Asymmetric Synthesis of cis-5-(Aminomethyl)-3-(4-methoxyphenyl)dihydrofuran-2(3H)- one

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초록

The asymmetric synthesis of (3R,5S )-5-(aminomethyl)-3-(4-methoxyphenyl)dihydrofuran-2(3 H )-one, as the most potent selective inactivator of monoamine B, was successfully achieved by applying a newly developed synthetic method toward the key -aminomethyl--lactone via intramolecular aziridine ring opening in 63% overall yield from a commercial starting material.

키워드

asymmetric synthesisgamma-aminomethyl--lactoneaziridinesring openingMONOAMINE-OXIDASE-BRING
제목
Asymmetric Synthesis of cis-5-(Aminomethyl)-3-(4-methoxyphenyl)dihydrofuran-2(3H)- one
저자
Kim, SonhwanLee, Won KooHa, Hyun-Joon
DOI
10.1055/s-0037-1610667
발행일
2019-02
유형
Article
저널명
Synthesis
51
4
페이지
885 ~ 888