INTRAMOLECULAR DIELS-ALDER REACTION OF SELENOALDEHYDES

被引：28

作者：

SEGI, M ^{[1
]}

TAKAHASHI, M ^{[1
]}

NAKAJIMA, T ^{[1
]}

SUGA, S ^{[1
]}

MURAI, S ^{[1
]}

SONODA, N ^{[1
]}

机构：

[1] OSAKA UNIV,FAC ENGN,DEPT APPL CHEM,SUITA,OSAKA 565,JAPAN

来源：

TETRAHEDRON LETTERS | 1988年 / 29卷 / 52期

关键词：

D O I：

10.1016/S0040-4039(00)88488-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：6965 / 6968

页数：4

共 14 条

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[2]

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[5]

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[6] REGIOCHEMICAL PREFERENCES IN SELENOALDEHYDE CYCLOADDITIONS [J].

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[7]

PAULMIER C, 1986, SELENIUM REAGENTS IN, P58

[8] STEREOCHEMICAL ASPECTS OF THE INTRAMOLECULAR DIELS-ALDER REACTIONS OF DECA-2,7,9-TRIENOATE ESTERS .3. THERMAL, LEWIS ACID-CATALYZED, AND ASYMMETRIC CYCLIZATIONS [J].

ROUSH, WR ;

GILLIS, HR ;

KO, AI .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (08) :2269-2283

[9] DIRECT CONVERSION OF ALDEHYDES TO SELENOALDEHYDES AND THIOALDEHYDES [J].

SEGI, M ;

NAKAJIMA, T ;

SUGA, S ;

MURAI, S ;

RYU, I ;

OGAWA, A ;

SONODA, N .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (06) :1976-1978

[10]

SEGI M, UNPUB

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