๐”– Bobbio Scriptorium
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The conversion of methyl pseudomonate C to pseudomonic acid A

โœ Scribed by Alan P. Kozikowski; Richard J. Schmiesing; Kirk L. Sorgi

Publisher
Elsevier Science
Year
1981
Tongue
French
Weight
171 KB
Volume
22
Category
Article
ISSN
0040-4039

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โœฆ Synopsis

summahy: A phoc&5b 6vh the conucuion 06 methyL pneudomanate C to pbeudamotic acid A tuLth pardid m..mwk.civ~q .LA debchibed.

๐Ÿ“œ SIMILAR VOLUMES

The structure and configuration of pseud
The structure and configuration of pseudomonic acid C
โœ J.Peter Clayton; Peter J. O'Hanlon; Norman H. Rogers ๐Ÿ“‚ Article ๐Ÿ“… 1980 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 228 KB

SUMHARY: A new antibiotic, pseudomonic aoid C (2a), has been isolated from fermentations

An approach to the synthesis of pseudomo
An approach to the synthesis of pseudomonic acids
โœ Ralph A. Raphael; John H.A. Stibbard; Raymond Tidbury ๐Ÿ“‚ Article ๐Ÿ“… 1982 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 139 KB

The synthesis of the cis-fused y-lactone 2,7-dioxabicycle-&3,4 non-4-en-g-one (3) by two routes is reported. Its stereoselective conversion to a key intermediate for pseudomonic acid synthesis is described.

A diastereocontrolled route to the tetra
A diastereocontrolled route to the tetrahydropyran nucleus of pseudomonic acids
โœ Takahiko Taniguchi; Kunio Ogasawara ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 64 KB

A diastereocontrolled synthesis of the tetrahydropyran nucleus of pseudomonic acids has been achieved starting from a chiral building block, which we have developed. The key step is a convex-face reduction of the block having a biased framework which allowed assemblage of the most important core in