STRUCTURES OF 2 7-MEMBERED RING PYRIMIDINE NUCLEOSIDE DERIVATIVES

被引:2
作者
SUTTON, PA
CODY, V
MARQUEZ, VE
机构
[1] MED FDN BUFFALO, 73 HIGH ST, BUFFALO, NY 14203 USA
[2] NCI, LPET, BETHESDA, MD 20205 USA
关键词
D O I
10.1080/07328318708069990
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Crystal structure analyses of 1-(2,3,5-tri-0-benzoyl-.beta.-D-ribofuranosyl)-tetrahydro-2H-1,3-diazepine-2,4(3H)-dione (I) and 1-(2,3,5-tri-0-benzoyl-.beta.-D-ribofuranosyl)-6,7-dihydro-2H-1,3-diazepine-2(3H)-one (II) show that the major conformational differences between them lie in the aglycone moiety. In I the aglycone is twisted with C(6) and C(7) above, and C(5) below, the plane of the ring. In II the aglycone has a sofa conformation with C(7) above the plane of the ring. The ribose conformation in both compounds is C(1'')-exo-C(2'')-endo (2T1), the C(4'')-C(5'') orientation is gauche-gauche, and the glycoside linkage is high-anti (X = -104.5(3).degree. I, -95.2(5.degree.) II, respectively).
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页码:613 / 620
页数:8
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