Title of article :
A short synthesis of the C15–C21 segment of (+)-discodermolide, based on an asymmetric approach from achiral 2-methyl-1,3-propanediol to versatile enantiopure stereotriads
Author/Authors :
Shahid، نويسنده , , Kazi A. and Li، نويسنده , , Yong-Nan and Okazaki، نويسنده , , Momotoshi and Shuto، نويسنده , , Yoshihiro and Goto، نويسنده , , Fumitaka and Kiyooka، نويسنده , , Syun-ichi، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2002
Pages :
4
From page :
6373
To page :
6376
Abstract :
A new approach was developed to versatile enantiopure stereotriads using chiral oxazaborolidinone-promoted asymmetric aldol reaction of a racemic aldehyde with a bromo silyl nucleophile. A short synthesis of the C15–C21 segment of (+)-discodermolide was achieved by elongation of one of the stereotriads with further diastereoselective aldol reaction with the same nucleophile.
Journal title :
Tetrahedron Letters
Serial Year :
2002
Journal title :
Tetrahedron Letters
Record number :
1653526
Link To Document :
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