NAGIOS: RODERIC FUNCIONANDO

Organocatalytic enantioselective Strecker reaction with seven-membered cyclic imines

Repositori DSpace/Manakin

dc.contributor.author	Lluna-Galán, Carles
dc.contributor.author	Blay Llinares, Gonzalo
dc.contributor.author	Fernández Picot, Isabel
dc.contributor.author	Muñoz, M. Carmen
dc.contributor.author	Pedro, José Ramón
dc.contributor.author	Vila Descals, Carlos
dc.date.accessioned	2020-03-27T09:57:19Z
dc.date.available	2020-03-27T09:57:19Z
dc.date.issued	2018
dc.identifier.citation	Lluna-Galán, Carles Blay Llinares, Gonzalo Fernández Picot, Isabel Muñoz, M. Carmen Pedro, José Ramón Vila Descals, Carlos 2018 Organocatalytic enantioselective Strecker reaction with seven-membered cyclic imines Advanced Synthesis & Catalysis 360 19 3662 3666
dc.identifier.uri	https://hdl.handle.net/10550/73682
dc.description.abstract	A highly enantioselective Strecker reaction with dibenzo[b,f][1,4]oxazepines has been described using a dihydroquinine-derived thiourea as organocatalyst. The reaction affords chiral 10,11-dihydrodibenzo[b,f][1,4]oxazepine 11-carbonitrile derivatives in excellent yields (up to 99%) and excellent enantioselectivities (up to 98%) under mild reaction conditions.
dc.language.iso	eng
dc.relation.ispartof	Advanced Synthesis & Catalysis, 2018, vol. 360, num. 19, p. 3662-3666
dc.subject	Catàlisi
dc.subject	Reaccions químiques
dc.title	Organocatalytic enantioselective Strecker reaction with seven-membered cyclic imines
dc.type	journal article	es_ES
dc.date.updated	2020-03-27T09:57:19Z
dc.identifier.doi	10.1002/adsc.201800754
dc.identifier.idgrec	127727
dc.rights.accessRights	open access	es_ES