REGIOSELECTIVE AND STEREOSELECTIVE ELECTROPHILIC ADDITIONS TO EXO AND ENDO-2-HYDROXY-2-METHYL-7-OXABICYCLO[2.2.1]HEPT-5-ENE

被引：12

作者：

ARJONA, O ^{[1
]}

DELAPRADILLA, RF ^{[1
]}

PEREZ, RA ^{[1
]}

PLUMET, J ^{[1
]}

VISO, A ^{[1
]}

机构：

[1] UNIV COMPLUTENSE MADRID,FAC QUIM,DEPT QUIM ORGAN,E-28040 MADRID,SPAIN

来源：

TETRAHEDRON LETTERS | 1987年 / 28卷 / 45期

关键词：

D O I：

10.1016/S0040-4039(00)96777-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

收藏

页码：5549 / 5550

页数：2

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[J]. TETRAHEDRON LETTERS, 1986, 27 (45) : 5505 - 5506
[2] STEREOSELECTIVITY OF THE REACTION BETWEEN 7-OXABICYCLO[2.2.1]HEPT-5-EN-2-ONE AND ORGANOCUPRATE REAGENTS
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PLUMET, J
[J]. TETRAHEDRON LETTERS, 1987, 28 (45) : 5547 - 5548
[3] REGIOSELECTIVITY OF ELECTROPHILIC ADDITIONS TO 7-OXABICYCLO[2.2.1]HEPTENES CONTROLLED BY REMOTE SUBSTITUENTS - ARENESULFONYL SUBSTITUTED 7-OXABICYCLO[2.2.1]HEPTENES AS STEREOSELECTIVE AND REGIOSELECTIVE CHIRAL DIENOPHILES
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1986, 51 (26) : 5341 - 5348
[4] NAKED SUGARS AS SYNTHETIC INTERMEDIATES - TOTAL SYNTHESIS OF L-DAUNOSAMINE
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1986, 51 (26) : 5348 - 5353