THE TOTAL SYNTHESIS OF (-)-INDOLIZIDINES 205A AND 235B

被引：16

作者：

SHISHIDO, Y ^{[1
]}

KIBAYASHI, C ^{[1
]}

机构：

[1] TOKYO COLL PHARM,HACHIOJI,TOKYO 19203,JAPAN

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1991年 / 18期

关键词：

D O I：

10.1039/c39910001237

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The total synthesis of (-)-indolizidines 205A and 235B, alkaloids from the arrow poison-frog, via a common chiral oxazino-lactam, prepared by an asymmetric intramolecular Diels-Alder reaction of an N-acylnitroso intermediate, is described.

引用

页码：1237 / 1239

页数：3

共 15 条

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[9] ENANTIODIVERGENT TOTAL SYNTHESIS OF NATURALLY-OCCURRING TRANS-2-BUTYL-5-PENTYLPYRROLIDINE
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[10] ENANTIOSELECTIVE TOTAL SYNTHESIS OF (+)-PYRROLIDINE AND (-)-PYRROLIDINE 197B, A NEW CLASS OF ALKALOID FROM THE DENDROBATID POISON FROG - ASSIGNMENT OF THE ABSOLUTE-CONFIGURATION
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