Title of article
An efficient stereoselective synthesis of (2S,4S,5R)-(−)-bulgecinine
Author/Authors
Krasi?ski، نويسنده , , Antoni and Jurczak، نويسنده , , Janusz، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2001
Pages
3
From page
2019
To page
2021
Abstract
N-Benzyl-N-carbobenzyloxy-O-tert-butyldimethylsilyl-d-serinal (6) was reacted under Barbier conditions with allyl bromide affording diastereoselectively (82:18) the anti-adduct 5, which was subsequently transformed into (2S,4S,5R)-(−)-bulgecinine (1).
Keywords
amino aldehydes , Asymmetric induction , epoxidation , cyclization , Pyrrolidines , allylation
Journal title
Tetrahedron Letters
Serial Year
2001
Journal title
Tetrahedron Letters
Record number
1643677
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