Highly diastereoselective Diels-Alder reactions of Baylis-Hillman adducts

VK Aggarwal; A Patin; S Tisserand

doi:10.1021/ol050584f

Highly diastereoselective Diels-Alder reactions of Baylis-Hillman adducts

VK Aggarwal^*, A Patin, S Tisserand

^*Corresponding author for this work

School of Chemistry

Research output: Contribution to journal › Article (Academic Journal) › peer-review

24 Citations (Scopus)

Abstract

Baylis-Hillman adducts were found to be excellent dienophiles in Diels-Alder reactions, providing essentially complete diastereocontrol (although mixtures of endolexo isomers) with all dienes.

Original language	English
Pages (from-to)	2555-2557
Number of pages	3
Journal	Organic Letters
Volume	7
Issue number	13
DOIs	https://doi.org/10.1021/ol050584f
Publication status	Published - 23 Jun 2005

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@article{f8642060b185417cab9f4a88a6baa23b,

title = "Highly diastereoselective Diels-Alder reactions of Baylis-Hillman adducts",

abstract = "Baylis-Hillman adducts were found to be excellent dienophiles in Diels-Alder reactions, providing essentially complete diastereocontrol (although mixtures of endolexo isomers) with all dienes.",

author = "VK Aggarwal and A Patin and S Tisserand",

year = "2005",

month = jun,

day = "23",

doi = "10.1021/ol050584f",

language = "English",

volume = "7",

pages = "2555--2557",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "13",

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TY - JOUR

T1 - Highly diastereoselective Diels-Alder reactions of Baylis-Hillman adducts

AU - Aggarwal, VK

AU - Patin, A

AU - Tisserand, S

PY - 2005/6/23

Y1 - 2005/6/23

N2 - Baylis-Hillman adducts were found to be excellent dienophiles in Diels-Alder reactions, providing essentially complete diastereocontrol (although mixtures of endolexo isomers) with all dienes.

AB - Baylis-Hillman adducts were found to be excellent dienophiles in Diels-Alder reactions, providing essentially complete diastereocontrol (although mixtures of endolexo isomers) with all dienes.

U2 - 10.1021/ol050584f

DO - 10.1021/ol050584f

M3 - Article (Academic Journal)

SN - 1523-7060

VL - 7

SP - 2555

EP - 2557

JO - Organic Letters

JF - Organic Letters

IS - 13

ER -

Highly diastereoselective Diels-Alder reactions of Baylis-Hillman adducts

Abstract

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