Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides (2003)
- Authors:
- USP affiliated authors: STEFANI, HELIO ALEXANDRE - FCF ; PETRAGNANI, NICOLA - IQ
- Unidades: FCF; IQ
- Subjects: SÍNTESE ORGÂNICA; QUÍMICA FARMACÊUTICA; FARMACOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Synthetic Communications
- ISSN: 0039-7911
- Volume/Número/Paginação/Ano: v. 33, n. 12, p. 2161-2166, 2003
-
ABNT
STEFANI, Hélio Alexandre et al. Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications, v. 33, n. 12, p. 2161-2166, 2003Tradução . . Acesso em: 19 set. 2024. -
APA
Stefani, H. A., Petragnani, N., Ascenso, M. F. C., & Zeni, G. (2003). Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications, 33( 12), 2161-2166. -
NLM
Stefani HA, Petragnani N, Ascenso MFC, Zeni G. Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications. 2003 ; 33( 12): 2161-2166.[citado 2024 set. 19 ] -
Vancouver
Stefani HA, Petragnani N, Ascenso MFC, Zeni G. Study toward the synthesis of selenofurans via seleno-Claisen rearrangement of allyl arylselenides. Synthetic Communications. 2003 ; 33( 12): 2161-2166.[citado 2024 set. 19 ] - Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides
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- Use of chiral sulfoxides in the asymmetric synthesis of pinellic acid methyl ester
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- Ciclização de compostos 2, 3 dicarbonilicos 2, 4-dialdienil substituidos
- Addition of organotellurenyl bromide to terminal acetylenes
- Iodine promoted cyclofunctionalization reaction of 2,4-dialkenyl-1,3-dicarbonyl compounds
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