Reaction of 4,6-0-benzylidene-3-0-mesyl-allal with allylic grignard reagents. Highly regio- and stereoselective preparation of 2,6-disubstituted dihydropyran rings-Reference-Cited by-同舟云学术

Reaction of 4,6-0-benzylidene-3-0-mesyl-allal with allylic grignard reagents. Highly regio- and stereoselective preparation of 2,6-disubstituted dihydropyran rings

Published:1983-01 Issue:33 Volume:24 Page:3505-3508
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ogihara Takuo,Mitsunobu Oyo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. 4,6-O-Benzylidene-3-deoxy-3-C-(iodomethyl)-D-allal: precursor of a cyclopropylcarbinyl-oxo-carbonium ion

2. Reaktionen von Acetylglycalen und Acetylpseudoglycalen mit Natriumsalzen unter Bortrifluorid‐Ätherat‐Katalyse

3. α-C-Glycopyranosides from Lewis acid catalysed condensations of acetylated glycals and enol silanes

4. Ultrasound in organic synthesis. 2. Formation and reaction of organocopper reagents

5. Nouvelle voie d'acces aux c-glycosides.

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