Synthesis of 7-Oxasphingosine and -ceramide Analogues and Their Evaluation in a Model for Apoptosis-Reference-Cited by-同舟云学术

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Synthesis of 7-Oxasphingosine and -ceramide Analogues and Their Evaluation in a Model for Apoptosis

Published:2004-11 Issue:11 Volume:1 Page:1785-1799
ISSN:1612-1872
Container-title:Chemistry & Biodiversity
language:en
Short-container-title:C&B

Author:

Rajan Roshini,Wallimann Kurt,Vasella Andrea,Pace Deborah,Genazzani Armando?A.,Canonico Pier?Luigi,Condorelli Fabrizio

Publisher

Wiley

Subject

Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering

Reference35 articles.

1. The cerebrosides

2. Bioorganic Chemistry of Ceramide

3. Designing anticancer drugs via the achilles heel: ceramide, allylic ketones, and mitochondria

4. Chemistry of glycosphingolipids—carbohydrate molecules of biological significance

5. Sphingosine kinase, sphingosine-1-phosphate, and apoptosis

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2. Stereoselective synthesis of higher homologues of pantolactone from (R)-glyceraldehyde acetonide;Tetrahedron Letters;2015-02

3. Enantioselective 6-endo bromoaminocyclization of 2,4-dienyl N-tosylcarbamates catalyzed by a chiral phosphine oxide-Sc(OTf)3 complex. A dramatic additive effect;Organic & Biomolecular Chemistry;2015

4. Glycal-Derived δ-Hydroxy α,β-Unsaturated Aldehydes (Perlin Aldehydes): Versatile Building Blocks in Organic Synthesis;Chemical Reviews;2013-02-18

5. 4,5,6-Trisubstituted Piperidinones as Conformationally Restricted Ceramide Analogues: Synthesis and Evaluation as Inhibitors of Sphingosine and Ceramide Kinases and as NKT Cell-Stimulatory Antigens;Chemistry & Biodiversity;2009-10

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