Core structure of eremophilanes and bakkanes through niobium catalyzed diels-alder reaction: synthesis of (+ OU -)-bakkenolide A (2006)
- Authors:
- USP affiliated authors: CONSTANTINO, MAURICIO GOMES - FFCLRP ; SILVA, GIL VALDO JOSE DA - FFCLRP
- Unidade: FFCLRP
- Subjects: CATALASE; NIÓBIO
- Language: Inglês
- Imprenta:
- Publisher place: Washington
- Date published: 2006
- Source:
- Título: Journal of Organic Chemistry
- ISSN: 0022-3263
- Volume/Número/Paginação/Ano: v. 71, p. 9880-9883, 2006
-
ABNT
CONSTANTINO, Maurício Gomes et al. Core structure of eremophilanes and bakkanes through niobium catalyzed diels-alder reaction: synthesis of (+ OU -)-bakkenolide A. Journal of Organic Chemistry, v. 71, p. 9880-9883, 2006Tradução . . Acesso em: 17 mar. 2026. -
APA
Constantino, M. G., Oliveira, K. T. de, Polo, E. C., Silva, G. V. J. da, & Brocksom, T. J. (2006). Core structure of eremophilanes and bakkanes through niobium catalyzed diels-alder reaction: synthesis of (+ OU -)-bakkenolide A. Journal of Organic Chemistry, 71, 9880-9883. -
NLM
Constantino MG, Oliveira KT de, Polo EC, Silva GVJ da, Brocksom TJ. Core structure of eremophilanes and bakkanes through niobium catalyzed diels-alder reaction: synthesis of (+ OU -)-bakkenolide A. Journal of Organic Chemistry. 2006 ; 71 9880-9883.[citado 2026 mar. 17 ] -
Vancouver
Constantino MG, Oliveira KT de, Polo EC, Silva GVJ da, Brocksom TJ. Core structure of eremophilanes and bakkanes through niobium catalyzed diels-alder reaction: synthesis of (+ OU -)-bakkenolide A. Journal of Organic Chemistry. 2006 ; 71 9880-9883.[citado 2026 mar. 17 ] - Stereochemistry in substituted cyclopentanes: an approach to the analysis by proton NMR
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- Fundamentos de química
- Niobium (V) chloride mediated preparation of 'beta'-chloro-'alfa','beta'-unsaturated ketones
- Síntese de 1-indanonas através da reação de acilação de Friedel-Crafts intramolecular utilizando 'NbCl IND.5' como ácido de Lewis
- An approach to the synthesis of furanoheliangolides through Diels-Alder reactions
- Principal component analysis of long-range 'W' coupling constants of some cyclic compounds
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