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  3. ASYMMETRIC HYDROXYLATION OF CHLOROPHYLL DERIVATIVES - A FACILE ENTRY TO BOTH DIASTEREOMERS OF CHLOROPHYLLONE A

ASYMMETRIC HYDROXYLATION OF CHLOROPHYLL DERIVATIVES - A FACILE ENTRY TO BOTH DIASTEREOMERS OF CHLOROPHYLLONE A

TitleASYMMETRIC HYDROXYLATION OF CHLOROPHYLL DERIVATIVES - A FACILE ENTRY TO BOTH DIASTEREOMERS OF CHLOROPHYLLONE A
Publication TypeJournal Article
Year of Publication1995
AuthorsMa, LF, Dolphin, D
JournalTetrahedron-Asymmetry
Volume6
Pagination313-316
Date PublishedFeb
Type of ArticleNote
ISBN Number0957-4166
Keywordsenol
Abstract

High stereoselectivity is observed for the asymmetric oxidation of chlorophyll enolates derived from 13(2),17(3)-pheophorbide a enol (3), pheophorbide a methyl ester (8) and pheophytin a (9) with DBU and N-sulfonyl oxaziridines (4), (5) and (6).
URL<Go to ISI>://A1995QK51400001