Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/15667

TitleHighly diastereoselective synthesis of 2-azabicyclo[2.2.1]hept-5-ene derivatives : bronsted acid catalized aza-diels-alder reaction between cyclopentadiene and imino-acetates with two chiral auxiliaries
Author(s)García-Mera, Xerardo
Rodríguez-Borges, José E.
Vale, M. Luísa C.
Alves, M. José
KeywordsAsymetric synthesis
Cycloadditions
Aza-Diels-Alder reaction
Induction
Chiral auxiliaries
Issue date2011
PublisherPergamon-Elsevier Science Ltd
JournalTetrahedron
Abstract(s)The cycloaddition between protonated glyoxylate imines possessing two chiral auxiliaries, N-(S)- or N-(R)-1-phenylethyl and (-)-8-phenylmenthyl or (+)-8- phenylneomenthyl, and cyclopentadiene is described. The absolute configuration of all adducts formed was unequivocally assigned through NMR, specific optical rotation and X-ray data of appropriated derivatives. Experimental results confirm the highly exoselectivity for these aza-Diels–Alder reactions, single adducts being obtained from combinations of (8PM)-(R-PEA) and (8PNM)-(S-PEA).
TypeArticle
URIhttp://hdl.handle.net/1822/15667
DOI10.1016/j.tet.2011.06.097
ISSN0040-4020
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CDQuim - Artigos (Papers)

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