A formal total synthesis of nikkomycin B based on enzymatic resolution of a primary alcohol possessing two stereogenic centers
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference5 articles.
1. The total synthesis of nikkomycin B
2. Applications of crotyldiisopinocampheylboranes in synthesis: the total synthesis of nikkomycin B
3. Stereoselective reduction of 2-methyl-3-oxo esters (or amides) with sodium borohydride catalyzed by manganese(II) chloride or tetrabutylammonium borohydride. A practical preparation of erythro and threo-3-hydroxy-2-methyl esters (or amides)
4. Stereoselective reduction of β-keto esters with zinc borohydride. stereoselective synthesis of -3-hydroxy-2-alkylpropionates
5. A highly stereoselective synthesis of the versatile chiral synthons possessing two stereogenic centers, the formal total syntheses of (−)-oudemansins A, B, and X
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1. ChemInform Abstract: A Formal Total Synthesis of Nikkomycin B Based on Enzymatic Resolution of a Primary Alcohol Possessing Two Stereogenic Centers.;ChemInform;2010-08-12
2. Optical Resolution, Biocatalysis;Encyclopedia of Industrial Biotechnology;2010-04-15
3. Biocatalysis Applied to the Synthesis of Agrochemicals;Current Organic Chemistry;2006-11-01
4. The stereoselective synthesis of α-substituted β-amino secondary alcohols based on the proline-mediated, asymmetric, three-component Mannich reaction and its application to the formal total synthesis of nikkomycins B and Bx;Tetrahedron;2005-11
5. Nucleoside Chemistry in Crop Protection;HETEROCYCLES;2005
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