Comparative Study for the Indroduction of a Masked Nucleophilic Acyl Moiety at the C(3) Site of alpha,beta-Unsaturated Aldehydes and Esters

Jean Lucchetti; Alain Krief

doi:10.1016/S0022-328X(00)96196-5

Comparative Study for the Indroduction of a Masked Nucleophilic Acyl Moiety at the C(3) Site of alpha,beta-Unsaturated Aldehydes and Esters

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Abstract

Bis(methylthio)- and bis(methylseleno)alkyllithiums in THF/HMPT (1.1 eq) and bis(phenylthio)alkyllithiums in DME were found to be the bes reagents out of several examined for formally introducing an acyl moiety at the C(3) site of α,β-unsaturated aldehydes and esters.

Original language	English
Pages (from-to)	C49-C52
Journal	Journal of Organometallic Chemistry
Volume	194
Issue number	3
DOIs	https://doi.org/10.1016/S0022-328X(00)96196-5
Publication status	Published - 1980

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@article{ce651bb1b76744e691c2e96784f83deb,

title = "Comparative Study for the Indroduction of a Masked Nucleophilic Acyl Moiety at the C(3) Site of alpha,beta-Unsaturated Aldehydes and Esters",

abstract = "Bis(methylthio)- and bis(methylseleno)alkyllithiums in THF/HMPT (1.1 eq) and bis(phenylthio)alkyllithiums in DME were found to be the bes reagents out of several examined for formally introducing an acyl moiety at the C(3) site of α,β-unsaturated aldehydes and esters.",

author = "Jean Lucchetti and Alain Krief",

year = "1980",

doi = "10.1016/S0022-328X(00)96196-5",

language = "English",

volume = "194",

pages = "C49--C52",

journal = "Journal of Organometallic Chemistry",

issn = "0022-328X",

publisher = "Elsevier",

number = "3",

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T1 - Comparative Study for the Indroduction of a Masked Nucleophilic Acyl Moiety at the C(3) Site of alpha,beta-Unsaturated Aldehydes and Esters

AU - Lucchetti, Jean

AU - Krief, Alain

PY - 1980

Y1 - 1980

N2 - Bis(methylthio)- and bis(methylseleno)alkyllithiums in THF/HMPT (1.1 eq) and bis(phenylthio)alkyllithiums in DME were found to be the bes reagents out of several examined for formally introducing an acyl moiety at the C(3) site of α,β-unsaturated aldehydes and esters.

AB - Bis(methylthio)- and bis(methylseleno)alkyllithiums in THF/HMPT (1.1 eq) and bis(phenylthio)alkyllithiums in DME were found to be the bes reagents out of several examined for formally introducing an acyl moiety at the C(3) site of α,β-unsaturated aldehydes and esters.

U2 - 10.1016/S0022-328X(00)96196-5

DO - 10.1016/S0022-328X(00)96196-5

M3 - Article

SN - 0022-328X

VL - 194

SP - C49-C52

JO - Journal of Organometallic Chemistry

JF - Journal of Organometallic Chemistry

IS - 3

ER -

Comparative Study for the Indroduction of a Masked Nucleophilic Acyl Moiety at the C(3) Site of alpha,beta-Unsaturated Aldehydes and Esters

Abstract

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