Lewis acid induced synthetic equivalents of imines and iminium ions.: Part 15.: Facile synthesis of β-anilinopropionates from Lewis acid-induced N-methyleneanilines with ketene acetals

Ha, HJ; Choi, CJ; Lee, WK

doi:10.1081/SCC-120004138

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Lewis acid induced synthetic equivalents of imines and iminium ions.: Part 15.: Facile synthesis of β-anilinopropionates from Lewis acid-induced N-methyleneanilines with ketene acetals

Ha, HJ;
Choi, CJ;
Lee, WK

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WEB OF SCIENCE

10

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SCOPUS

12

초록

A facile synthesis of beta-anilinopropionates was achieved from the reaction of N-methyleneanilines derived from 1,3,5-triphenylhexahydro-1,3,5-triazines with ketene acetals in the presence of Lewis acid.

키워드

INTERMOLECULAR POLAR <4-PI(+)+2-PI>-CYCLOADDITIONS; METHYLENEAMINE EQUIVALENTS; DIASTEREOSELECTIVE SYNTHESIS; CATIONIC 2-AZABUTADIENES; 1,2,3,4-TETRAHYDROQUINOLINES; HEXAHYDRO-1,3,5-TRIAZINES

제목: Lewis acid induced synthetic equivalents of imines and iminium ions.: Part 15.: Facile synthesis of β-anilinopropionates from Lewis acid-induced N-methyleneanilines with ketene acetals

저자: Ha, HJ; Choi, CJ; Lee, WK

DOI: 10.1081/SCC-120004138

발행일: 2002

유형: Article

저널명: Synthetic Communications

권: 32

호: 10

페이지: 1495 ~ 1500