The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction (2009)
- Authors:
- USP affiliated authors: SANTOS, ALCINDO APARECIDO DOS - IQ ; COMASSETO, JOAO VALDIR - IQ
- Unidades: IQ; IQ
- DOI: 10.1016/j.tetlet.2009.09.023
- Subjects: SÍNTESE ORGÂNICA; QUÍMICA ORGÂNICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Tetrahedron Letters
- ISSN: 0040-4039
- Volume/Número/Paginação/Ano: v. 50, n. 47, p. 6498-6501, 2009
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
SILVA, Márcio S.; SANTOS, Alcindo Aparecido dos; COMASSETO, João Valdir. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, Oxford, v. 50, n. 47, p. 6498-6501, 2009. DOI: 10.1016/j.tetlet.2009.09.023. -
APA
Silva, M. S., Santos, A. A. dos, & Comasseto, J. V. (2009). The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters, 50( 47), 6498-6501. doi:10.1016/j.tetlet.2009.09.023 -
NLM
Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501. -
Vancouver
Silva MS, Santos AA dos, Comasseto JV. The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction. Tetrahedron Letters. 2009 ; 50( 47): 6498-6501. - Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones
- Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts
- Tellurium in organic synthesis: a general approach to buteno- and butanolides
- A new approach to organomanganese compounds: the tellurium/manganese exchange reaction
- Selenium-stabilized carbanions
- A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides
- Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi
- Tellurium in organic synthesis: a new approach to trisubstituted 'gama'-butyrolactones with trans-trans relative stereochemistry. Total enantioselective synthesis of (-)-Blastmycinolactol, (+)-Blastmycinone, (-)-NFX-2, and (+)-Antimycinone
- Synthesis of pheromones through C-alkylation using Te/Li exchange and transmetallation reactions
- Enzimatic resolution of 'gamma'-hydroxy vinylic tellurides: route to chiral lactones
Informações sobre o DOI: 10.1016/j.tetlet.2009.09.023 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
