SYNTHESIS OF ANTITUMOR ANSAMYCINS .2. A FORMAL SYNTHESIS OF (+/-)-MACBECIN-I

被引:16
作者
COUTTS, SJ [1 ]
KALLMERTEN, J [1 ]
机构
[1] SYRACUSE UNIV,DEPT CHEM,SYRACUSE,NY 13244
关键词
D O I
10.1016/S0040-4039(00)97607-X
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Convergent synthesis of (±)-2 a key intermediate in the Merck synthesis of macbecin I (1.), incorporates the chelation-mediated coupling of a lithiated aryl subunit and the γ-hydroxy aldehyde equivalent 8 to establish a critical connective element of the parent ansamycin. © 1990.
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页码:4305 / 4308
页数:4
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