Simple Tandem Olefin Isomerization/Intramolecular Hydroamination of Alkenyl Amines with Various Allylic Tethers

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3
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SCOPUS

3

초록

A simple and efficient AgOTf-promoted tandem olefin isomerization/intramolecular hydroamination of 1,1-disub-stituted alkenyl amines has been developed. This one-pot process represents a facile and attractive route for the synthesis of diverse 2-alkyl-substituted 1,3-X,N-heterocycles through chemo-and regiose-lective C(sp3)-N bond formation with atom economy. Advantages such as the operationally simple and practical procedure that uses a readily available catalyst under aerobic conditions, good to excellent chemical yields, the high functional group tolerance, the broad substrate scope, and high efficiency and selectivity are noteworthy.

키워드

CATALYZED INTRAMOLECULAR HYDROAMINATION; O-BOND FORMATIONS; SEQUENTIAL C-C; OXAZOLIDINE DERIVATIVES; TRIFLIC ACID; ISOMERIZATION/CYCLIZATION; PHENOLS; SYSTEM; REARRANGEMENT; HETEROCYCLES
제목
Simple Tandem Olefin Isomerization/Intramolecular Hydroamination of Alkenyl Amines with Various Allylic Tethers
저자
Kim, Young Ho; Bin Kim, Dong; Youn, So Won
DOI
10.1021/acs.joc.2c01640
발행일
2022-09
유형
Article
저널명
The Journal of Organic Chemistry
권
87
호
17
페이지
11919 ~ 11924