SYNTHESIS OF THE ENANTIOMERS OF 1,7-DIOXASPIRO[5.5]UNDECANE AND 4-HYDROXY 1,7-DIOXASPIRO[5.5]UNDECANE, THE COMPONENTS OF THE OLIVE FLY PHEROMONE

被引：33

作者：

MORI, K ^{[1
]}

UEMATSU, T ^{[1
]}

WATANABE, H ^{[1
]}

YANAGI, K ^{[1
]}

MINOBE, M ^{[1
]}

机构：

[1] SUMITOMO CHEM CO LTD,TAKATSUKI RES INST,OSAKA 569,JAPAN

来源：

TETRAHEDRON LETTERS | 1984年 / 25卷 / 35期

关键词：

D O I：

10.1016/S0040-4039(01)91192-X

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：3875 / 3878

页数：4

共 16 条

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[6] WOOL WAX .6. THE SYNTHESIS AND STEREOCHEMISTRY OF THE STRAIGHT-CHAIN ALPHA-HYDROXY-ACIDS
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[7] CHIRAL REAGENTS FROM TARTARIC ACID - 1-BENZYLOXY-3,4-EPOXY-2-BUTANOL, A VERSATILE INTERMEDIATE FOR THE SYNTHESIS OF ENANTIOMERS
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[8] N,N,N',N'-TETRAMETHYLPHOSPHORODIAMIDATE GROUP - USEFUL FUNCTION FOR PROTECTION OR REDUCTIVE DEOXYGENATION OF ALCOHOLS AND KETONES
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (14) : 5098 - &
[9] SPIROKETALS - THE SYNTHESIS OF AN OLIVE FLY PHEROMONE COMPONENT, 4-HYDROXY-1,7-DIOXASPIRO[5,5]UNDECANE, VIA A NOVEL CATION-OLEFIN CYCLIZATION STEP
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[J]. TETRAHEDRON LETTERS, 1983, 24 (52) : 5915 - 5918
[10] A NEW SYNTHESIS OF 1,7-DIOXASPIRO[5.5]UNDECANES - APPLICATION TO A RECTAL GLAND SECRETION OF THE OLIVE FRUIT-FLY (DACUS-OLEAE)
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