A NEW SYNTHESIS OF GAMMA-SUBSTITUTED ALPHA-METHYLENE-GAMMA-BUTYROLACTONES (2-METHYLENE-4-ALKANOLIDES) USING CATALYSIS BY SNCL2/AMBERLYST-15

被引：0

作者：

TALAGA, P ^{[1
]}

SCHAEFFER, M ^{[1
]}

BENEZRA, C ^{[1
]}

STAMPF, JL ^{[1
]}

机构：

[1] UNIV LOUIS PASTEUR,CHU STRASBOURG,DERMATOL CLIN,CNRS,DERMATOCHIM LAB,F-67091 STRASBOURG,FRANCE

来源：

SYNTHESIS-STUTTGART | 1990年 / 06期

关键词：

D O I：

暂无

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：530 / 530

页数：1

共 41 条

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TETRAHEDRON LETTERS, 1986, 27 (14) : 1561 - 1562
[35] NEW METHOD FOR THE SYNTHESIS OF 2-SUBSTITUTED 2-BUTEN-4-OLIDE VIA ALPHA-SUBSTITUTED "BETA-PHENYLTHIO-GAMMA-BUTYROLACTONE
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[36] Simple synthesis of trans-alpha,beta-dibenzyl-gamma-butyrolactone lignans by diastereoselective reduction of alpha-benzylidene-beta-benzyl-gamma-butyrolactones using NaBH4-NiCl2
Moritani, Y
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Miyagishima, T
Ohmizu, H
Iwasaki, T
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1996, 69 (08) : 2281 - 2286
[37] SYNTHESIS OF 2-PENTEN-4-OLIDES, 3-PENTEN-4-OLIDES, AND 4,4-DIALKYL-1,3-CYCLOPENTANEDIONES BY ACID-INDUCED AND BASE-INDUCED ISOMERIZATION OF 4-PENTEN-4-OLIDES (GAMMA-METHYLENE-GAMMA-BUTYROLACTONES)
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SYNTHESIS-STUTTGART, 1986, (11): : 921 - 925
[38] NEW METHODS FOR STEREOSELECTIVE SYNTHESIS OF ALPHA-ALKYLIDENE-GAMMA-BUTYROLACTONES USING MONOANION OF O-ETHYL S-(TETRAHYDRO-2-OXO-3-FURANYL) THIOCARBONATE AND DIANION OF ALPHA-MERCAPTO-GAMMA-BUTYROLACTONE
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BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1980, 53 (10) : 2910 - 2916
[39] SYNTHESIS AND BIOLOGICAL-ACTIVITY OF SUBSTITUTED ALPHA,ALPHA'[IMINO BIS(METHYLENE)]-BIS-[3,4 DIHYDRO-2H-1-BENZOPYRAN-2-METHANOLS] - A NEW CLASS OF ANTIHYPERTENSIVE COMPOUNDS
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DEBRUYN, M
SCHROVEN, M
PHARMACEUTISCH WEEKBLAD-SCIENTIFIC EDITION, 1988, 10 (06) : 301 - 301
[40] Potential antitumor alpha-methylene-gamma-butyrolactone-bearing nucleic acid bases .2. Synthesis of 5'-methyl-5'-[2-(5-substituted uracil-1-yl)ethyl]-2'-oxo-3'-methylenetetrahydrofurans
Kim, JC
Kim, JA
Park, JI
Kim, SH
Kim, SH
Choi, SK
Park, WW
ARCHIVES OF PHARMACAL RESEARCH, 1997, 20 (03) : 253 - 258

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