A novel method for deprotection of N-9-phenylfluoren-9-yl group using iodine catalyst: Simple synthesis of (2S, 3R, 4R)-3,4-dihydroxyproline

Citation
Jh. Kim et al., A novel method for deprotection of N-9-phenylfluoren-9-yl group using iodine catalyst: Simple synthesis of (2S, 3R, 4R)-3,4-dihydroxyproline, SYNLETT, (5), 1999, pp. 614-616
Citations number
18
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNLETT
ISSN journal
09365214 → ACNP
Issue
5
Year of publication
1999
Pages
614 - 616
Database
ISI
SICI code
0936-5214(199905):5<614:ANMFDO>2.0.ZU;2-Z
Abstract
Iodine was found to he an efficient catalyst for the deprotection of the N- phenylfluoren-9-yl (Pf) group in tertiary amine and promote an intramolecul ar amination. A facile and economical synthesis of (2S,3R,4R)-3,4-dihydroxy proline was accomplished via iodine promoted cyclization and deprotection.