Lewis acid-mediated [3+2] cycloaddition of allyltriisopropylsilane to N-sulfonyl aldimines

Authors
Akiyama, T Sugano, M Kagoshima, H
Citation
T. Akiyama et al., Lewis acid-mediated [3+2] cycloaddition of allyltriisopropylsilane to N-sulfonyl aldimines, TETRAHEDR L, 42(23), 2001, pp. 3889-3892
Citations number
36
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
42
Issue
23
Year of publication
2001
Pages
3889 - 3892
Database
ISI
SICI code
0040-4039(20010604)42:23<3889:LA[COA>2.0.ZU;2-0
Abstract
BF3. OEt2-mediated [3+2] cycloaddition of allyltriisopropylsilane to N-sulf onyl aldimine afforded silyl substituted pyrrolidines in good yields. Excel lent cis selectivity was observed with aromatic aldimines. (C) 2001 Elsevie r Science Ltd. All rights reserved.