Diastereo-controlled Diels–Alder cycloadditions of erythrose benzylidene-acetal 1,3-butadienes by 4-substituted-1,2,4-triazoline-3,5-dione: Evidence for the stereoelectronic effects on the dienes-Reference-Cited by-同舟云学术

Diastereo-controlled Diels–Alder cycloadditions of erythrose benzylidene-acetal 1,3-butadienes by 4-substituted-1,2,4-triazoline-3,5-dione: Evidence for the stereoelectronic effects on the dienes

Published:2010-08 Issue:15 Volume:21 Page:1817-1820
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Alves Maria J.,Duarte Vera C.M.,Faustino Hélio,Fortes António Gil

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference11 articles.

1. Asymmetric Diels–Alder reactions. Part 3. Influence of butadiene structure upon the diastereofacial reactivity of (E)-1-(2′,3′,4′,6′-tetra-O-acetyl-β-D-glucopyranosyloxy)buta-1,3-dienes

2. Enhanced discrimination by aza dienophiles over their olefinic counterparts for the diastereotopic faces of methyl (E,E)-5-(2′,3′,4′,6′-tetra-O-acetyl-β-d-glucopyranosyloxy)penta-2,4-dienoate

3. Asymmetric synthesis of (3S)-2,3,4,5-tetrahydropyridazine-3-carboxylic acid

4. Diels-Alder reaction of in-situ generated 2-methoxycarbonyl-p-quinone with D-glucose based dienes: A new approach to forskolin

5. Synthesis of leukotriene A4 methyl ester from D-glucose

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4. Total Facial Discrimination of 1,3-Dipolar Cycloadditions in a d-Erythrose 1,3-Dioxane Template: Computational Studies of a Concerted Mechanism;The Journal of Organic Chemistry;2017-01-09

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