DSpace university logo mark
Advanced Search
Japanese | English 

NAOSITE : Nagasaki University's Academic Output SITE > School of Pharmaceutical Sciences > Articles in academic journal >

Regioselective Introduction of Electrophiles into Piperidine Derivatives at the 4-Position

File Description SizeFormat
Heterocycles76_177.pdf134.58 kBAdobe PDFView/Open

Title: Regioselective Introduction of Electrophiles into Piperidine Derivatives at the 4-Position
Authors: Onomura, Osamu / Fujimura, Noriyuki / Oda, Takahisa / Matsumura, Yoshihiro / Demizu, Yosuke
Issue Date: Sep-2008
Publisher: Japan Institute of Heterocyclic Chemistry
Citation: Heterocycles, 76(1), pp.177-182; 2008
Abstract: Regioselective introduction of various electrophiles (aldehydes, ketones, and imines) into piperidine skeleton at the 4-position was achieved with a catalytic amount of Pd(OAc)2/PPh3 in the presence of excess Et2Zn. In addition, enantioselective introduction of benzaldehyde into piperidine derivatives was accomplished by using chiral phosphine ligand with moderate enantioselectivity.
URI: http://hdl.handle.net/10069/21989
ISSN: 03855414
DOI: 10.3987/COM-08-S(N)26
Rights: Copyright © 2008 The Japan Institute of Heterocyclic Chemistry
Type: Journal Article
Text Version: author
Appears in Collections:Articles in academic journal

Citable URI : http://hdl.handle.net/10069/21989

All items in NAOSITE are protected by copyright, with all rights reserved.


Valid XHTML 1.0! Copyright © 2006-2015 Nagasaki University Library - Feedback Powerd by DSpace