SYNTHETIC STUDY OF USTILOXIN ANALOGS - BENZYLIC OXIDATION OF 13-MEMBERED CYCLIC PEPTIDE BY LEAD-TETRAACETATE

Authors
TAKAHASHI M SHIRAI R KOISO Y IWASAKI S
Citation
M. Takahashi et al., SYNTHETIC STUDY OF USTILOXIN ANALOGS - BENZYLIC OXIDATION OF 13-MEMBERED CYCLIC PEPTIDE BY LEAD-TETRAACETATE, Heterocycles, 47(1), 1998, pp. 163-166
Citations number
15
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Heterocycles → ACNP
ISSN journal
03855414
Volume
47
Issue
1
Year of publication
1998
Pages
163 - 166
Database
ISI
SICI code
0385-5414(1998)47:1<163:SSOUA->2.0.ZU;2-4
Abstract
The 13-membered cyclic peptides (5, 6), analogs of phomopsin-ustiloxin class of antibiotics, have been synthesized. Benzylic hydroxyl group was introduced in desired stereochemistry by lead tetraacetate oxidati on followed by methanolysis.