Trimethylsilyl-Halide-Mediated Conjugated Addition to Allylic Acetals

Bernard Feringa

doi:10.1080/00397918508076812

Trimethylsilyl-Halide-Mediated Conjugated Addition to Allylic Acetals

Bernard Feringa

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Trimethylsilyl chloride can effect the conjugated addition of NaX (X = Br, I, SCN) to α,β-unsaturated acetals and ketals without deprotection of the carbonyl group.

Originele taal-2	English
Aantal pagina's	3
Tijdschrift	Synthetic Communications
Volume	15
Nummer van het tijdschrift	2
DOI's	https://doi.org/10.1080/00397918508076812
Status	Published - 1985

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title = "Trimethylsilyl-Halide-Mediated Conjugated Addition to Allylic Acetals",

abstract = "Trimethylsilyl chloride can effect the conjugated addition of NaX (X = Br, I, SCN) to α,β-unsaturated acetals and ketals without deprotection of the carbonyl group.",

author = "Bernard Feringa",

note = "Relation: http://www.rug.nl/scheikunde/ date_submitted:2005 Rights: University of Groningen. Stratingh Institute",

year = "1985",

doi = "10.1080/00397918508076812",

language = "English",

volume = "15",

journal = "Synthetic Communications",

publisher = "Marcel Dekker",

number = "2",

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T1 - Trimethylsilyl-Halide-Mediated Conjugated Addition to Allylic Acetals

AU - Feringa, Bernard

N1 - Relation: http://www.rug.nl/scheikunde/ date_submitted:2005 Rights: University of Groningen. Stratingh Institute

PY - 1985

Y1 - 1985

N2 - Trimethylsilyl chloride can effect the conjugated addition of NaX (X = Br, I, SCN) to α,β-unsaturated acetals and ketals without deprotection of the carbonyl group.

AB - Trimethylsilyl chloride can effect the conjugated addition of NaX (X = Br, I, SCN) to α,β-unsaturated acetals and ketals without deprotection of the carbonyl group.

U2 - 10.1080/00397918508076812

DO - 10.1080/00397918508076812

M3 - Article

VL - 15

JO - Synthetic Communications

JF - Synthetic Communications

IS - 2

ER -