Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone (2004)
- Authors:
- USP affiliated authors: COMASSETO, JOAO VALDIR - IQ
- Unidades: IQ
- Subjects: QUÍMICA ORGÂNICA; SÍNTESE ORGÂNICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Synthetic Communications
- ISSN: 0039-7911
- Volume/Número/Paginação/Ano: v. 34, n. 5, p. 817-828, 2004
-
ABNT
CLOSOSKI, Giuliano Cesar; COSTA, Carlos E.; MISSIO, Lauri João; CASS, Quezia Bezerra; COMASSETO, João Valdir. Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications, New York, v. 34, n. 5, p. 817-828, 2004. -
APA
Clososki, G. C., Costa, C. E., Missio, L. J., Cass, Q. B., & Comasseto, J. V. (2004). Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications, 34( 5), 817-828. -
NLM
Clososki GC, Costa CE, Missio LJ, Cass QB, Comasseto JV. Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications. 2004 ; 34( 5): 817-828. -
Vancouver
Clososki GC, Costa CE, Missio LJ, Cass QB, Comasseto JV. Enzymatic resolution of 5-phenylselanyltetrahydro-2-furanone. Enantioselective preparation of (R) and (S)-gamma-valerolactone. Synthetic Communications. 2004 ; 34( 5): 817-828. - Sintese de um tetranorditerpeno
- Synthesis of diarylselenides and diarylsulfides under phase transfer conditions
- Adicao de selenofenol a sistemas insaturados
- Química orgânica sintética
- Adicao de anions de telurio a acetilenos
- Use of aminoiminothanesulfinic acid ( thiourea dioxide) under phase transfer conditions for generating organochalcogenate anions. Synthesis of sulfides , selenides and tellurides
- Divulgacao do conhecimento cientifico no brasil
- Acetylenic tellurides: sunthesis and reactivity
- Synthesis of 1- chloro -1-alken-1-yl selenides ( chlorovinyl selenides )
- 1,3- carbonyl transposition with chain elongation
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