Synthetic microbial chemistry, XV. Synthesis of (2E,4R,5S,11R)-(−)-Cladospolide A, a Phytotoxic Macrolide fromCladosporium cladosporioides
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Reference27 articles.
1. Synthesis of both enantiomers of 9-ethyl-1,7-dioxaspiro[5.5]-undecan-4-one, the key intermediate in the synthesis of talaromycins A and B.
2. Structure of cladospolide A, a novel macrolide from Cladosporium fulvum.
3. New plant growth regulators, cladospolide A and B, macrolides produced by Cladosporium cladosporioides.
4. Absolute stereochemistry of cladospolide A, a phytotoxic macrolide from Cladosporium cladosporioides.
5. Absolute Stereostructure Determination of Cladospolide A Using MTPA Ester Method
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