THE ELECTRON-RELEASING HOMOCONJUGATED CARBONYL GROUP - APPLICATION TO THE TOTAL SYNTHESES OF 3-DEOXY-, 4-DEOXY-HEXOSE, LIVIDOSAMINE AND DERIVATIVES

被引：27

作者：

FATTORI, D ^{[1
]}

DEGUCHTENEERE, E ^{[1
]}

VOGEL, P ^{[1
]}

机构：

[1] UNIV LAUSANNE,INST CHIM ORGAN,2 RUE BARRE,CH-1005 LAUSANNE,SWITZERLAND

来源：

TETRAHEDRON LETTERS | 1989年 / 30卷 / 52期

关键词：

D O I：

10.1016/S0040-4039(00)70712-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：7415 / 7418

页数：4

共 37 条

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[6] THE CARBONYL GROUP AS HOMOCONJUGATED ELECTRON-RELEASING SUBSTITUENT - REGIOSELECTIVE ELECTROPHILIC ADDITIONS AT BICYCLO[2.2.1]HEPT-5-EN-2-ONE, BICYCLO[2.2.2]OCT-5-EN-2-ONE AND DERIVATIVES [J].

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[9] REGIOSELECTIVE ADDITIONS OF ELECTROPHILES TO OLEFINS REMOTELY PERTURBED - THE CARBONYL GROUP AS A HOMOCONJUGATED ELECTRON DONATING SUBSTITUENT [J].

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[10]

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