Synthesis of a cyclic diaryl ether derivative under solid-phase conditions

Authors
Nakamura, K Nishiya, H Nishiyama, S
Citation
K. Nakamura et al., Synthesis of a cyclic diaryl ether derivative under solid-phase conditions, TETRAHEDR L, 42(36), 2001, pp. 6311-6313
Citations number
10
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
42
Issue
36
Year of publication
2001
Pages
6311 - 6313
Database
ISI
SICI code
0040-4039(20010903)42:36<6311:SOACDE>2.0.ZU;2-N
Abstract
The TTN phenolic oxidation, along with the N-protective group of the corres ponding tripeptide derivatives, was examined to accomplish construction of a cyclic isodityrosine derivative under solid-phase conditions. The desired cyclization was effected under the TTN (thallium(III) trinitrate)/NMP-MeOH conditions to give the corresponding 17-membered ring lactam 12. (C) 2001 Elsevier Science Ltd. All rights reserved.