Stereoselective synthesis of methyl branched chiral deoxypropionate units: a new route for synthesis of insect pheromone (−)-lardolure and (2R,4R,6R,8R) 2,4,6,8-tetramethylundecanoic acid-Reference-Cited by-同舟云学术

Stereoselective synthesis of methyl branched chiral deoxypropionate units: a new route for synthesis of insect pheromone (−)-lardolure and (2R,4R,6R,8R) 2,4,6,8-tetramethylundecanoic acid

Published:2012-10 Issue:44 Volume:53 Page:5952-5954
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Yadav J.S.,Sengupta Sandip,Yadav Nagendra Nath,Narasimha Chary D.,Al Ghamdi Ahmad Alkhazim

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. Application of Conformation Design in Acyclic Stereoselection: Total Synthesis of Borrelidin as the Crystalline Benzene Solvate

2. Total Synthesis of Ionomycin Using Ring-Opening Strategies

3. Efficient and Selective Synthesis of Siphonarienolone and Related Reduced Polypropionates via Zr-Catalyzed Asymmetric Carboalumination

4. The total synthesis of (+)-pectinatone: An iterative alkylation approach based on the SAMP-hydrazone method

5. Total Synthesis of (+)-Bourgeanic Acid Utilizing Desymmetrization Strategy

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