A stereocontrolled route to d-ribo-phytosphingosine and sphinganine from an achiral secondary homoallylic alcohol using Sharpless kinetic resolution-Reference-Cited by-同舟云学术

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A stereocontrolled route to d-ribo-phytosphingosine and sphinganine from an achiral secondary homoallylic alcohol using Sharpless kinetic resolution

Published:2013-05 Issue:19 Volume:69 Page:3817-3822
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Devi Thongam Joymati,Saikia Bishwajit,Barua Nabin C.

Funder

Council of Scientific and Industrial Research, India

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference65 articles.

1. Studies on sphingosines, XIV. On the phytosphingosine content of the major human kidney glycolipids

2. Phytosphingosines and branched sphingosines in kidney

3. Phytosphingosine kills Candida albicans by disrupting its cell membrane

4. Sphingolipid targets in cancer therapy

5. Regulation of γ-Secretase Activity in Alzheimer's Disease

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1. A simple approach to novel 1,3-diamino-1,3-dideoxydihydrosphingosines;Tetrahedron Letters;2024-05

2. Rh(i)-catalyzed site-selective hydroacylation of alkenyl-bearing allylic alcohols with non-chelating aldehydes controlled by in situ generated carbonyl group;New Journal of Chemistry;2022

3. Sharpless Asymmetric Epoxidation: Applications in the Synthesis of Bioactive Natural Products;Mini-Reviews in Organic Chemistry;2021-07-27

4. Synthesis and Biological Activity of 2-(2-Amino-2-phenylethyl)-5-oxotetrahydrofuran-2-carboxylic Acid: A Microwave-Assisted 1,3-Dipolar Cycloaddition Approach;Synlett;2021-07-27

5. Stereoselective synthesis and antiproliferative activity of the isomeric sphinganine analogues;Carbohydrate Research;2019-01

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