October 14, 1987Liebigs Annalen der Chemie

Synthetic microbial chemistry, XV. Synthesis of (2E,4R,5S,11R)‐(−)‐Cladospolide A, a Phytotoxic Macrolide from Cladosporium cladosporioides

View Full Paper

Ask AI

Bookmark

Abstract

The total synthesis of cladospolide A [(2E,4R,5S,11R)‐4,5‐dihydroxy‐2‐dodecen‐11‐olide (1a)] was achieved in 16 steps from ethyl (R)‐3‐hydroxybutanoate (2a).

Discussion

No takes yet. Share an insight, caveat, or question.

Cite This Study

Mori et al. (1987) studied this question.

synapsesocial.com/papers/6a9377cb904295c54c2cc8ba https://doi.org/10.1002/jlac.198719870841

View Full Paper

Ask AI

Bookmark

Abstract

The total synthesis of cladospolide A [(2E,4R,5S,11R)‐4,5‐dihydroxy‐2‐dodecen‐11‐olide (1a)] was achieved in 16 steps from ethyl (R)‐3‐hydroxybutanoate (2a).

Synthetic microbial chemistry, XV. Synthesis of (2E,4R,5S,11R)‐(−)‐Cladospolide A, a Phytotoxic Macrolide from Cladosporium cladosporioides

Abstract

Discussion

Cite This Study

Synthetic microbial chemistry, XV. Synthesis of (2E,4R,5S,11R)‐(−)‐Cladospolide A, a Phytotoxic Macrolide from Cladosporium cladosporioides

Abstract

Discussion

Cite This Study

Keep reading

Keep reading