Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts (2012)
- Authors:
- USP affiliated authors: COMASSETO, JOAO VALDIR - IQ ; SANTOS, ALCINDO APARECIDO DOS - IQ
- Unidade: IQ
- DOI: 10.1016/j.tet.2012.09.027
- Subjects: COMPOSTOS ORGANOMETÁLICOS; CALCOGÊNIOS
- Language: Inglês
- Imprenta:
- Source:
- Título: Tetrahedron
- ISSN: 0040-4020
- Volume/Número/Paginação/Ano: v. 68, n. 51, p. 10406-10413, 2012
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
SOUSA, Bruno Artur de et al. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts. Tetrahedron, v. 68, n. 51, p. 10406-10413, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2012.09.027. Acesso em: 02 out. 2024. -
APA
Sousa, B. A. de, Keppler, A. F., Gariani, R. A., Comasseto, J. V., & Santos, A. A. dos. (2012). Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts. Tetrahedron, 68( 51), 10406-10413. doi:10.1016/j.tet.2012.09.027 -
NLM
Sousa BA de, Keppler AF, Gariani RA, Comasseto JV, Santos AA dos. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts [Internet]. Tetrahedron. 2012 ; 68( 51): 10406-10413.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tet.2012.09.027 -
Vancouver
Sousa BA de, Keppler AF, Gariani RA, Comasseto JV, Santos AA dos. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts [Internet]. Tetrahedron. 2012 ; 68( 51): 10406-10413.[citado 2024 out. 02 ] Available from: https://doi.org/10.1016/j.tet.2012.09.027 - The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction
- Selenium-stabilized carbanions
- A new approach to organomanganese compounds: the tellurium/manganese exchange reaction
- Tellurium in organic synthesis: a general approach to buteno- and butanolides
- Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones
- 'Alpha'-trimethylsilyl-'gamma'-hydroxy-tellurides: A route to reactive C-O-vinyl dianions
- Enzymatic kinetic of resolution of alkynylic hydroxyesters
- The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2
- Reactive organometallics from organotellurides: application in organic synthesis
- Solventless and mild procedure to prepare organotellurium(IV) compounds under microwave irradiation
Informações sobre o DOI: 10.1016/j.tet.2012.09.027 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas