Synthesis of 2,6-cis-disubstituted 4-methylenetetrahydropyrans by oxy-Michael addition

Duncan Gill; Nicholas H. Taylor; Eric J. Thomas

doi:10.1016/j.tet.2011.03.113

Synthesis of 2,6-cis-disubstituted 4-methylenetetrahydropyrans by oxy-Michael addition

Duncan Gill
, Nicholas H. Taylor
, Eric J. Thomas

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

Abstract

The combination of an 'ene' reaction between a 2-(2-trialkylsilyloxyalkyl) prop-2-enyl(trimethyl)silane and an alk-1-yn-3-one mediated by zinc(II) iodide, and an intramolecular oxy-Michael reaction, provides an efficient synthesis of cis-2,6-disubstituted 4-methylenetetrahydropyrans of interest in the context of a synthesis of bryostatins. The stereoselective formation of (E)-vinylsilanes in the 'ene' reaction is of interest. © 2011 Elsevier Ltd. All rights reserved.

Original language	English
Pages (from-to)	5034-5045
Number of pages	11
Journal	Tetrahedron
Volume	67
Issue number	27-28
DOIs	https://doi.org/10.1016/j.tet.2011.03.113
Publication status	Published - 8 Jul 2011

Keywords

4-Methylenetetrahydropyran
Allyl silane
Ene reactions
oxy-Michael addition
Vinyl silane

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10.1016/j.tet.2011.03.113

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title = "Synthesis of 2,6-cis-disubstituted 4-methylenetetrahydropyrans by oxy-Michael addition",

abstract = "The combination of an 'ene' reaction between a 2-(2-trialkylsilyloxyalkyl) prop-2-enyl(trimethyl)silane and an alk-1-yn-3-one mediated by zinc(II) iodide, and an intramolecular oxy-Michael reaction, provides an efficient synthesis of cis-2,6-disubstituted 4-methylenetetrahydropyrans of interest in the context of a synthesis of bryostatins. The stereoselective formation of (E)-vinylsilanes in the 'ene' reaction is of interest. {\textcopyright} 2011 Elsevier Ltd. All rights reserved.",

keywords = "4-Methylenetetrahydropyran, Allyl silane, Ene reactions, oxy-Michael addition, Vinyl silane",

author = "Duncan Gill and Taylor, \{Nicholas H.\} and Thomas, \{Eric J.\}",

year = "2011",

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day = "8",

doi = "10.1016/j.tet.2011.03.113",

language = "English",

volume = "67",

pages = "5034--5045",

journal = "Tetrahedron",

issn = "0040-4020",

publisher = "Elsevier BV",

number = "27-28",

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TY - JOUR

T1 - Synthesis of 2,6-cis-disubstituted 4-methylenetetrahydropyrans by oxy-Michael addition

AU - Gill, Duncan

AU - Taylor, Nicholas H.

AU - Thomas, Eric J.

PY - 2011/7/8

Y1 - 2011/7/8

N2 - The combination of an 'ene' reaction between a 2-(2-trialkylsilyloxyalkyl) prop-2-enyl(trimethyl)silane and an alk-1-yn-3-one mediated by zinc(II) iodide, and an intramolecular oxy-Michael reaction, provides an efficient synthesis of cis-2,6-disubstituted 4-methylenetetrahydropyrans of interest in the context of a synthesis of bryostatins. The stereoselective formation of (E)-vinylsilanes in the 'ene' reaction is of interest. © 2011 Elsevier Ltd. All rights reserved.

AB - The combination of an 'ene' reaction between a 2-(2-trialkylsilyloxyalkyl) prop-2-enyl(trimethyl)silane and an alk-1-yn-3-one mediated by zinc(II) iodide, and an intramolecular oxy-Michael reaction, provides an efficient synthesis of cis-2,6-disubstituted 4-methylenetetrahydropyrans of interest in the context of a synthesis of bryostatins. The stereoselective formation of (E)-vinylsilanes in the 'ene' reaction is of interest. © 2011 Elsevier Ltd. All rights reserved.

KW - 4-Methylenetetrahydropyran

KW - Allyl silane

KW - Ene reactions

KW - oxy-Michael addition

KW - Vinyl silane

U2 - 10.1016/j.tet.2011.03.113

DO - 10.1016/j.tet.2011.03.113

M3 - Article

SN - 0040-4020

VL - 67

SP - 5034

EP - 5045

JO - Tetrahedron

JF - Tetrahedron

IS - 27-28

ER -

Synthesis of 2,6-cis-disubstituted 4-methylenetetrahydropyrans by oxy-Michael addition

Abstract

Keywords

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