Reductive transformations with trimethylsilyl chloride-sodium iodide. A new synthesis of 4H-1,3-oxazines

Eugene Ghera; Rakesh Maurya; Alfred Hassner

doi:10.1016/s0040-4039(01)80790-5

Reductive transformations with trimethylsilyl chloride-sodium iodide. A new synthesis of 4H-1,3-oxazines

Eugene Ghera
, Rakesh Maurya
, Alfred Hassner

Department of Chemistry

Bar-Ilan University

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

18 Scopus citations

Abstract

1-Arylalkenes and 1-arylalkanols are reduced to arylalkanes on heating with trimethylsilyl chloride/sodium iodide in CH₃CN. Under similar conditions enones, dialkylated in the β-position of the double bond, give 4H-1,3-oxazines.

Original language	English
Pages (from-to)	4741-4744
Number of pages	4
Journal	Tetrahedron Letters
Volume	30
Issue number	35
DOIs	https://doi.org/10.1016/s0040-4039(01)80790-5
State	Published - 1989

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title = "Reductive transformations with trimethylsilyl chloride-sodium iodide. A new synthesis of 4H-1,3-oxazines",

abstract = "1-Arylalkenes and 1-arylalkanols are reduced to arylalkanes on heating with trimethylsilyl chloride/sodium iodide in CH3CN. Under similar conditions enones, dialkylated in the β-position of the double bond, give 4H-1,3-oxazines.",

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AU - Maurya, Rakesh

AU - Hassner, Alfred

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N2 - 1-Arylalkenes and 1-arylalkanols are reduced to arylalkanes on heating with trimethylsilyl chloride/sodium iodide in CH3CN. Under similar conditions enones, dialkylated in the β-position of the double bond, give 4H-1,3-oxazines.

AB - 1-Arylalkenes and 1-arylalkanols are reduced to arylalkanes on heating with trimethylsilyl chloride/sodium iodide in CH3CN. Under similar conditions enones, dialkylated in the β-position of the double bond, give 4H-1,3-oxazines.

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JO - Tetrahedron Letters

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IS - 35

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Reductive transformations with trimethylsilyl chloride-sodium iodide. A new synthesis of 4H-1,3-oxazines

Abstract

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