A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides (2009)
- Authors:
- USP affiliated authors: SANTOS, ALCINDO APARECIDO DOS - IQ ; COMASSETO, JOAO VALDIR - IQ
- Unidade: IQ
- DOI: 10.1016/j.tetasy.2009.10.009
- Subjects: SÍNTESE ORGÂNICA; LÍTIO; COMPOSTOS ORGÂNICOS
- Language: Inglês
- Imprenta:
- Source:
- Título: Tetrahedron: Asymmetry
- ISSN: 0957-4166
- Volume/Número/Paginação/Ano: v. 20, n. 23, p. 2699-2703, 2009
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
PRINCIVAL, Jefferson Luiz et al. A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides. Tetrahedron: Asymmetry, v. 20, n. 23, p. 2699-2703, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2009.10.009. Acesso em: 10 fev. 2026. -
APA
Princival, J. L., Oliveira, M. S. C. de, Santos, A. A. dos, & Comasseto, J. V. (2009). A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides. Tetrahedron: Asymmetry, 20( 23), 2699-2703. doi:10.1016/j.tetasy.2009.10.009 -
NLM
Princival JL, Oliveira MSC de, Santos AA dos, Comasseto JV. A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 23): 2699-2703.[citado 2026 fev. 10 ] Available from: https://doi.org/10.1016/j.tetasy.2009.10.009 -
Vancouver
Princival JL, Oliveira MSC de, Santos AA dos, Comasseto JV. A large-scale synthesis of enantiomerically pure gamma-hydroxy-organochalcogenides [Internet]. Tetrahedron: Asymmetry. 2009 ; 20( 23): 2699-2703.[citado 2026 fev. 10 ] Available from: https://doi.org/10.1016/j.tetasy.2009.10.009 - Functionalized organozincates and organocuprates derived from 'gama'-hydroxytellurides in the preparation of 1,4-hydroxyketones
- Reactive organometallics from organotellurides: application in organic synthesis
- The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2
- 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
- 'Alpha'-trimethylsilyl-'gamma'-hydroxy-tellurides: A route to reactive C-O-vinyl dianions
- Selenium-stabilized carbanions
- A new approach to organomanganese compounds: the tellurium/manganese exchange reaction
- Enzymatic kinetic of resolution of alkynylic hydroxyesters
- Tellurium in organic synthesis: the enantioselective synthesis of the pheromone blend components of Mayetiola destructor, Drosophila mulleri and Contarinia pisi
- The soft nucleophilicity of organotellurolates driving the 'S IND. N' 2-type lactone ring-opening reaction
Informações sobre o DOI: 10.1016/j.tetasy.2009.10.009 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
