STEREOCHEMICAL STUDY ON THE CYCLO-ADDITION OF A CYCLIC NITRONE TO 5-METHYL-2(5H)-FURANONE

被引：20

作者：

FIGUEREDO, M ^{[1
]}

FONT, J ^{[1
]}

DEMARCH, P ^{[1
]}

机构：

[1] UNIV AUTONOMA BARCELONA,DEPT QUIM,UNITAT QUIM ORGAN,E-08193 BARCELONA,SPAIN

来源：

CHEMISCHE BERICHTE | 1989年 / 122卷 / 09期

关键词：

D O I：

10.1002/cber.19891220916

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1701 / 1704

页数：4

共 34 条

[1] REACTIVITY, REGIOCHEMISTRY, AND STEREOCHEMISTRY OF A CYCLIC NITRONE AND ITS ALPHA-KETO DERIVATIVE IN 1, 3-DIPOLAR CYCLO-ADDITION REACTIONS
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[2] THE REGIOCHEMISTRY AND STEREOCHEMISTRY OF 1,3-DIPOLAR CYCLO-ADDITION OF A CYCLIC NITRONE
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WAZEER, MIM
[J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1988, (03): : 597 - 605
[3] REGIO-SELECTIVE AND FACE-SELECTIVE 1,3-DIPOLAR CYCLO-ADDITIONS TO LEVOGLUCOSENONE
BLAKE, AJ
FORSYTH, AC
PATON, RM
[J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1988, (06) : 440 - 442
[4] STERIC EFFECTS VS SECONDARY ORBITAL INTERACTIONS IN NITRONE CYCLO-ADDITIONS - STERIC EFFECTS IN CYCLOREVERSIONS OF ISOXAZOLIDINES
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OBERTI, R
[J]. TETRAHEDRON, 1988, 44 (12) : 3735 - 3748
[5] ALKYLATION OF (1S,2R,5R,6S,7R)- AND (1R,2R,5R,6S,7S)-5-METHYL-4-OXATRICYCLO-[5.2.1.0/2,6]-8-DECEN-3-ONE - APPLICATION TO THE SYNTHESIS OF (R)-3-ALKYL-5-METHYL-2(5H)-FURANONES
CORBERA, J
FONT, J
MONSALVATJE, M
ORTUNO, RM
SANCHEZFERRANDO, F
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (18) : 4393 - 4395
[6] ASYMMETRIC 1,3-DIPOLAR CYCLO-ADDITIONS TO 5-MENTHYLOXY-2[5H]-FURANONES
DELANGE, B
FERINGA, BL
[J]. TETRAHEDRON LETTERS, 1988, 29 (41) : 5317 - 5320
[7] PSEUDOESTERS AND DERIVATIVES .24. 1,3-DIPOLAR CYCLOADDITION OF DIAZOMETHANE TO 5-METHOXYFURAN-2(5H)-ONES
FARINA, F
MARTIN, MV
SANCHEZ, F
[J]. HETEROCYCLES, 1986, 24 (09) : 2587 - 2592
[8] 1,3-DIPOLAR CYCLOADDITIONS ON HETEROCYCLES .17. STEREOSELECTIVITY OF CYCLOADDITIONS OF ARYLNITRILE OXIDES TO 5-ALKOXY-2(5H)-FURANONE
FISERA, L
ORAVEC, P
[J]. COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, 1987, 52 (05) : 1315 - 1324
[9] SYNTHESIS OF GEM-DIMETHYLCYCLOPROPANES BY MEANS OF 2-DIAZOPROPANE
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[J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1968, 7 (01) : 65 - &
[10] FRANCKNEUMANN M, 1968, ANGEW CHEM, V80, P42

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