Synthesis of enantiomerically pure 2,3-dideoxy-hept-2-enono-1,4-lactone derivatives diastereoselective addition of 2-(trimethylsiloxy)furan to -glyceraldehyde and -serinal-based three-carbon synthons-Reference-Cited by-同舟云学术

Synthesis of enantiomerically pure 2,3-dideoxy-hept-2-enono-1,4-lactone derivatives diastereoselective addition of 2-(trimethylsiloxy)furan to -glyceraldehyde and -serinal-based three-carbon synthons

Published:1989-01 Issue:39 Volume:30 Page:5325-5328
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Casiraghi Giovanni,Colombo Lino,Rassu Gloria,Spanu Pietro

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. An investigation of the use of l-ascorbic acid and its derivatives in the synthesis of spirodilactones

2. Synthesis of the enantiomers of 4-substituted γ-lactones with known absolute configuration

3. The structure of leptosphaerin

4. Marine natural products

5. Diels-alder cycloadditions of chiral butenolides with butadiene and isoprene:diastereofacial selectivity and regioselectivity

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