STEREOSELECTIVE SYNTHESIS OF (1R,3R,5S)-1,3-DIMETHYL-2,9-DIOXABICYCLO[3.3.1]NONANE

被引：30

作者：

NAKATA, T

NAGAO, S

TAKAO, S

TANAKA, T

OISHI, T

机构：

来源：

TETRAHEDRON LETTERS | 1985年 / 26卷 / 01期

关键词：

D O I：

10.1016/S0040-4039(00)98470-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

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页码：73 / 74

页数：2

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[5] STUDIES DIRECTED TOWARD THE TOTAL SYNTHESIS OF STREPTOGRAMIN ANTIBIOTICS - ENANTIOSPECIFIC APPROACH TO THE 9-MEMBERED MACROCYCLE OF GRISEOVIRIDIN
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[6] STEREOSELECTIVE SYNTHESIS OF THE FUNCTIONALIZED SYN-1,3,5,7-TETRAOL
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[7] REDLICH H, 1983, LIEBIGS ANN CHEM, P393
[8] OPEN-CHAIN SUGAR DITHIOACETALS AS COMPONENTS IN SYNTHESIS OF NATURAL SUBSTANCES .3. SYNTHESIS OF 4 ISOMERIC 1,3-DIMETHYL-2,9-DIOXALRICYCLO(3,3,1)NONANES FROM D-GLUCOSE
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[9] A SIMPLE STEREOSELECTIVE SYNTHESIS OF (1R,3R,5S)-1,3-DIMETHYL-2,9-DIOXA-BICYCLO[3,3,1]NONANE USING REGIOSELECTIVE RING-OPENING OF (R)-BETA-METHYL-BETA-PROPIOLACTONE
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[J]. CHEMISTRY LETTERS, 1983, (09) : 1391 - 1392