A new entry to functionalized cycloalkylamines: diastereoselective intramolecular amidoalkylation of N,O-acetal TMS ether possessing allylsilane

Jung, JW; Shin, DY; Seo, SY; Kim, SH; Paek, SM; Jung, JK; Suh, YG

doi:10.1016/j.tetlet.2004.11.136

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A new entry to functionalized cycloalkylamines: diastereoselective intramolecular amidoalkylation of N,O-acetal TMS ether possessing allylsilane

Jung, JW;
Shin, DY;
Seo, SY;
Kim, SH;
Paek, SM;
외 2명

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WEB OF SCIENCE

22

Citations

SCOPUS

24

초록

Highly diastereoselective cyclization (>20:1) as a new entry to functionalized cycloalkylamines has been conducted with acyclic N,O-acetal TMS ethers possessing an allylsilane moiety. (C) 2004 Elsevier Ltd. All rights reserved.

키워드

cycloalkylamine; intramolecular amidoalkylation; N,O-acetal; TMS ether; N-ACYLIMINIUM IONS; VERSATILE CONVERSION; BETA-PEPTIDES; CYCLOCONDENSATION; PRECURSOR; AMIDES

제목: A new entry to functionalized cycloalkylamines: diastereoselective intramolecular amidoalkylation of N,O-acetal TMS ether possessing allylsilane

저자: Jung, JW; Shin, DY; Seo, SY; Kim, SH; Paek, SM; Jung, JK; Suh, YG

DOI: 10.1016/j.tetlet.2004.11.136

발행일: 2005-01-24

유형: Article

저널명: Tetrahedron Letters

권: 46

호: 4

페이지: 573 ~ 575