STUDIES ON THE SYNTHESES OF LACTONES .15. SYNTHESES OF 4 POSSIBLE DIASTEREOISOMERS OF BOHLMANN STRUCTURE OF ISOEPOXYESTAFIATIN - THE STEREOCHEMICAL ASSIGNMENT OF ISOEPOXYESTAFIATIN

被引：19

作者：

ANDO, M ^{[1
]}

YOSHIMURA, H ^{[1
]}

机构：

[1] TOHOKU UNIV,FAC SCI,DEPT CHEM,AOBA KU,SENDAI,MIYAGI 980,JAPAN

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1993年 / 58卷 / 15期

关键词：

D O I：

10.1021/jo00067a056

中图分类号：

O62 [有机化学];

学科分类号：

070303 [有机化学]; 081704 [应用化学];

摘要：

The stereochemistry of isoepoxyestafiatin was determined to be 1beta,10beta:3alpha,4alpha-diepoxyguaia-11(13)-eno-12,6alpha-lactone by the syntheses of the four possible diastereoisomers 23-26.

引用

页码：4127 / 4131

页数：5

共 5 条

[1]

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ANDO, M ;

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[2]

STUDIES ON THE SYNTHESES OF SESQUITERPENE LACTONES .8. SYNTHESES OF SAUSSUREA LACTONE, 8-DEOXYMELITENSIN, AND 11,12-DEHYDRO-8-DEOXYMELITENSIN VIA A NOVEL FRAGMENTATION REACTION [J].

ANDO, M ;

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TAKASE, K .

JOURNAL OF ORGANIC CHEMISTRY, 1983, 48 (08) :1210-1216

[3]

Ando M., 1992, YUKI GOSEI KAGAKU KY, V50, P858

[4]

BOHLMANN F, 1972, TETRAHEDRON LETT, P621

[5]

REAPPRAISAL OF THE STEREOCHEMISTRY OF ELECTROPHILIC ADDITIONS TO 3-NORCARENES - X-RAY AND H-1-NMR ANALYSIS OF NORCARENE EPOXIDE CONFORMATION - ROLE OF MAGNETIC ANISOTROPIC CONTRIBUTIONS OF EPOXIDE RINGS [J].

PAQUETTE, LA ;

FRISTAD, WE ;

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BENO, MA ;

CHRISTOPH, GG .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1979, 101 (16) :4645-4655

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