Title of article :
Studies toward the total synthesis of irumamycin: stereoselective preparation of the C(15)–C(27) segment via two-directional chain synthesis
Author/Authors :
Hirose، نويسنده , , Tomoyasu and Sunazuka، نويسنده , , Toshiaki and Yamamoto، نويسنده , , Daisuke and Mouri، نويسنده , , Mutsumi and Hagiwara، نويسنده , , Yoshiaki and Matsumaru، نويسنده , , Takanori and Kaji، نويسنده , , Eisuke and ?mura، نويسنده , , Satoshi، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2007
Pages :
4
From page :
413
To page :
416
Abstract :
The basic structure of the C(15)–C(27) part of irumamycin (1) was synthesized. Stereoselective assembly of C16, 17, 22, and an extra C21 stereocenter was achieved by two-directional Brown’s asymmetric allyl boration. Group selective PMP acetal formation and oxidative cleavage of vinyl group facilitated the differentiation of the ends of a two-directionally synthesized chain.
Journal title :
Tetrahedron Letters
Serial Year :
2007
Journal title :
Tetrahedron Letters
Record number :
1853954
Link To Document :
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