Stereospecific synthesis of 5,6-dihydro-2H-pyran system. High-pressure cycloaddition of 1:2,3:4-di-0-isopropylidene- α-D-galactopyranose-6-ulose to 1-methoxybuta-1,3-diene-Reference-Cited by-同舟云学术

Stereospecific synthesis of 5,6-dihydro-2H-pyran system. High-pressure cycloaddition of 1:2,3:4-di-0-isopropylidene- α-D-galactopyranose-6-ulose to 1-methoxybuta-1,3-diene

Published:1984 Issue:42 Volume:25 Page:4809-4812
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Jurczak Janusz,Bauer Tomasz,Jarosz Sławomir

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. Organic Syntheses under High Pressure; I. High-Pressure Diels-Alder Reactions between 1-Methoxybuta-1,3-diene and Carbonyl Compounds

2. Resolution and absolute configuration of trans (+)- and (−)-6-hydroxymethyl-2-methoxy-5,6-dihydro-2H-pyrans, substrates for total synthesis of monosaccharides

3. The synthesis of 3,6-diamino-2,3,4,6-tetradeoxy-dl-threo-hexopyranose derivatives, substrates for the synthesis of negamycin

4. Organic syntheses under high pressure. 3. General approach to the synthesis of naturally occurring .delta.-lactones

5. Asymmetric induction in the high-pressure cycloaddition of 2,3-O-isopropylidene-D-glyceraldehyde to 1-methoxybuta-1,3-diene

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