'Alpha'-trimethylsilyl-'gamma'-hydroxy-tellurides: A route to reactive C-O-vinyl dianions (2009)
- Authors:
- USP affiliated authors: SANTOS, ALCINDO APARECIDO DOS - IQ ; COMASSETO, JOAO VALDIR - IQ
- Unidade: IQ
- Assunto: SÍNTESE ORGÂNICA
- Language: Inglês
- Imprenta:
- Publisher: UFSCar
- Publisher place: São Carlos
- Date published: 2009
- Source:
- Título: Abstracts
- Conference titles: Brazilian Meeting on Organic Synthesis - BMOS
-
ABNT
PRINCIVAL, Jefferson Luiz e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. 'Alpha'-trimethylsilyl-'gamma'-hydroxy-tellurides: A route to reactive C-O-vinyl dianions. 2009, Anais.. São Carlos: UFSCar, 2009. . Acesso em: 23 jan. 2025. -
APA
Princival, J. L., Santos, A. A. dos, & Comasseto, J. V. (2009). 'Alpha'-trimethylsilyl-'gamma'-hydroxy-tellurides: A route to reactive C-O-vinyl dianions. In Abstracts. São Carlos: UFSCar. -
NLM
Princival JL, Santos AA dos, Comasseto JV. 'Alpha'-trimethylsilyl-'gamma'-hydroxy-tellurides: A route to reactive C-O-vinyl dianions. Abstracts. 2009 ;[citado 2025 jan. 23 ] -
Vancouver
Princival JL, Santos AA dos, Comasseto JV. 'Alpha'-trimethylsilyl-'gamma'-hydroxy-tellurides: A route to reactive C-O-vinyl dianions. Abstracts. 2009 ;[citado 2025 jan. 23 ] - The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction
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- 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
- Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones
- 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
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