The orientation of the β-hydroxyl group controls the diastereoselectivity during the hydride reduction and Grignard reaction of inososes-Reference-Cited by-同舟云学术

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The orientation of the β-hydroxyl group controls the diastereoselectivity during the hydride reduction and Grignard reaction of inososes

Published:2013-06 Issue:25 Volume:69 Page:5144-5151
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Jagdhane Rajendra C.,Patil Madhuri T.,Krishnaswamy Shobhana,Shashidhar Mysore S.

Funder

Department of Science and Technology, New Delhi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference58 articles.

1. Chemistry of Inositol Lipid Mediated Cellular Signaling

2. Phosphoinositides: Chemistry, Biochemistry and Biomedical Applications,1999

3. Cell Signalling;Hancock,2005

4. Photoactivatable and Cell-Membrane-Permeable Phosphatidylinositol 3,4,5-Trisphosphate

5. Regioselective Protection and Deprotection of Inositol Hydroxyl Groups

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3. Useful access to enantiomerically pure protected inositols from carbohydrates: the aldohexos-5-uloses route;Beilstein Journal of Organic Chemistry;2016-11-08

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