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The stereoselective synthesis of 4-formyltrinem, a key intermediate for novel trinems

โœ Scribed by Chiara Ghiron; Tino Rossi; Russell J. Thomas


Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
209 KB
Volume
38
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


The stereoselective synthesis of a protected 4-fonnyltrinem 8 was accomplished in good yield. This connpound is a I~tenlial intermediate in the synthesis of a wide range of 4-alkyl and alkenyl substituted trineua antibiotics, as evidenced by its reaction with a series of phosphoranes and phosphonatcs.


๐Ÿ“œ SIMILAR VOLUMES


ChemInform Abstract: The Stereoselective
โœ C. GHIRON; T. ROSSI; R. J. THOMAS ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 31 KB ๐Ÿ‘ 3 views

The Stereoselective Synthesis of 4-Formyltrinem, a Key Intermediate for Novel Trinems. -Title compound (VIII) is a key intermediate for the preparation of a wide range of trinem derivatives. This is demonstrated by performing some Wittig reactions.

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