Synthesis of optically active 1,3-dioxin-4-one derivatives having a hydroxymethyl group at the 2-position and their use for regio-, diastereo-, and enantioselective synthesis of substituted cyclobutanols-Reference-Cited by-同舟云学术

Synthesis of optically active 1,3-dioxin-4-one derivatives having a hydroxymethyl group at the 2-position and their use for regio-, diastereo-, and enantioselective synthesis of substituted cyclobutanols

Published:2003-01 Issue:2 Volume:14 Page:201-215
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Murakami Masayuki,Kamaya Hiroshi,Kaneko Chikara,Sato Masayuki

Publisher

Elsevier BV

Subject

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

Reference27 articles.

1. Totally stereoselective additions to 2,6-disubstituted 1,3-dioxin-4-ones (chiral acetoacetic acid derivatives). Synthetic and mechanistic aspects of remote stereoselectivity

2. Asymmetric Photocycloadditions with Optically Pure, Spirocyclic Enones. Simple Synthesis of (+)- and (−)-Grandisol

3. Cycloadditions, 53. New spirocyclic chiral dienes — synthesis and diastereoselective Diels-Alder reactions withN-phenylmaleimide

4. Photocycloaddition, methylation, and catalytic reduction of chiral spirocyclic 1,3-dioxin-4-ones: Different stereofacial selectivity and its explanation.

5. Synthesis of 1,3-dioxin-4-ones and their use in synthesis. XVII. Chiral spirocyclic 4-oxo-1,3-dioxin-5-carboxylates. Asymmetric synthesis of carbocyclic C-nucleoside precursors.

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