Efficient regioselective syntheses of α and β cuparenones. A new approach for the construction of the cyclopentane ring

S. Halazy, F. Zutterman, A. Krief

Research output: Contribution to journal › Article › peer-review

Abstract

This paper discloses the regioselective synthesis of the cyclopentane ring from a carbonyl compound via two ring expension reactions.

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title = "Efficient regioselective syntheses of α and β cuparenones. A new approach for the construction of the cyclopentane ring",

abstract = "This paper discloses the regioselective synthesis of the cyclopentane ring from a carbonyl compound via two ring expension reactions.",

author = "S. Halazy and F. Zutterman and A. Krief",

year = "1982",

month = jan,

day = "1",

language = "English",

volume = "23",

pages = "4385--4388",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "42",

}

TY - JOUR

T1 - Efficient regioselective syntheses of α and β cuparenones. A new approach for the construction of the cyclopentane ring

AU - Halazy, S.

AU - Zutterman, F.

AU - Krief, A.

PY - 1982/1/1

Y1 - 1982/1/1

N2 - This paper discloses the regioselective synthesis of the cyclopentane ring from a carbonyl compound via two ring expension reactions.

AB - This paper discloses the regioselective synthesis of the cyclopentane ring from a carbonyl compound via two ring expension reactions.

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M3 - Article

AN - SCOPUS:0001509786

SN - 0040-4039

VL - 23

SP - 4385

EP - 4388

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 42

ER -