Stereoselective synthesis and biological activity of β- and α-D-arabinose 1,5-diphosphate: Analogues of a potent metabolic regulator

DOI: 10.1021/ja00337a034

Source and publish data:

Journal of the American Chemical Society p. 7851 - 7853 (1984)

Update date:2022-09-26

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Authors:

Maryanoff

Reitz Reitz

Tutwiler

et al. et al.

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Article abstract of DOI:10.1021/ja00337a034

Full text of DOI:10.1021/ja00337a034

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Article Doi

Stereoselective synthesis and biological activity of β- and α-D-arabinose 1,5-diphosphate: Analogues of a potent metabolic regulator

DOI: 10.1021/ja00337a034

Source and publish data:

Authors:

Article abstract of DOI:10.1021/ja00337a034

Full text of DOI:10.1021/ja00337a034

Products guided by the article

R&D Labs maybe for 93041-21-5

Relevant to this article

Synthesis, anti-cancer evaluation of benzenesulfonamide derivatives as potent tubulin-targeting agents

STEREO- AND REGIOSELECTIVITY IN IODO DIOL FORMATION FROM ACYCLIC ALLYLIC ALCOHOLS

Realized C-H functionalization of aryldiazo compounds via rhodium relay catalysis

Asymmetric synthesis of 3-oxa-15-deoxy-16-(m-tolyl)-17,18,19,20- tetranorisocarbacyclin and its neuroprotective analogue 15-deoxy-16-(m-tolyl)- 17,18,19,20-tetranorisocarbacyclin based on the conjugate addition-azoalkene- asymmetric olefination strategy

A Novel Approach to the Synthesis of the Cannabinoids

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