Synthesis of a C1-C14 subunit of the macrodiolide antibiotics pamamycin-607 and pamamycin-635B

DOI: 10.1016/0040-4039(95)00471-N

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Tetrahedron Letters p. 3091 - 3094 (1995)

Update date:2022-08-04

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Walkup Walkup

Kim Kim

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Article abstract of DOI:10.1016/0040-4039(95)00471-N

A nonracemic C₁-C₁₄ portion of the antibiotics pamamycin-607 and -635B was prepared using a route which features two stereoselective aldol reactions (including an apparent kinetic resolution via the Evans aldol reaction), a stereospe

Full text of DOI:10.1016/0040-4039(95)00471-N

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Article Doi

Synthesis of a C1-C14 subunit of the macrodiolide antibiotics pamamycin-607 and pamamycin-635B

DOI: 10.1016/0040-4039(95)00471-N

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0040-4039(95)00471-N

Full text of DOI:10.1016/0040-4039(95)00471-N

Products guided by the article

R&D Labs maybe for 164413-26-7

Relevant to this article

Intramolecular catalytic Friedel-Crafts reactions with allenyl cations for the synthesis of quinolines and their analogues

An efficient synthesis of 3-substituted isoquinoline and pyridine derivatives by gold catalyzed intramolecular cyclization from o-alkynyloximes

Heterocyclization of derivatives of 4-oxoalkanoic acids to 1,5-disubstituted pyrrolin-2-ones

Facial Selectivity in Cycloadditions of a Chiral Ketene Acetal under Microwave Irradiation in Solvent-Free Conditions. Configurational Assignment of the Cycloadducts by NOESY Experiments and Molecular Mechanics Calculations