Detailed 1H and 13C NMR structural assignment and relative stereochemistry determination for three new and one known semi-synthetic sesquiterpene lactones (2012)
- Authors:
- USP affiliated authors: LOPES, JOAO LUIS CALLEGARI - FCFRP ; CONSTANTINO, MAURICIO GOMES - FFCLRP
- Unidades: FCFRP; FFCLRP
- DOI: 10.1016/j.molstruc.2011.11.012
- Subjects: QUÍMICA ORGÂNICA; PRODUTOS NATURAIS; RESSONÂNCIA MAGNÉTICA NUCLEAR (MÉTODOS)
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of Molecular Structure
- ISSN: 0022-2860
- Volume/Número/Paginação/Ano: v. 1008, p. 24-28, 2012
- Status:
- Artigo possui versão em acesso aberto em repositório (Green Open Access)
- Versão do Documento:
- Versão submetida (Pré-print)
- Acessar versão aberta:
-
ABNT
SASS, Daiane Cristina et al. Detailed 1H and 13C NMR structural assignment and relative stereochemistry determination for three new and one known semi-synthetic sesquiterpene lactones. Journal of Molecular Structure, v. 1008, p. 24-28, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2011.11.012. Acesso em: 09 maio 2026. -
APA
Sass, D. C., Heleno, V. C. G., Soares, A. C. F., Lopes, J. L. C., & Constantino, M. G. (2012). Detailed 1H and 13C NMR structural assignment and relative stereochemistry determination for three new and one known semi-synthetic sesquiterpene lactones. Journal of Molecular Structure, 1008, 24-28. doi:10.1016/j.molstruc.2011.11.012 -
NLM
Sass DC, Heleno VCG, Soares ACF, Lopes JLC, Constantino MG. Detailed 1H and 13C NMR structural assignment and relative stereochemistry determination for three new and one known semi-synthetic sesquiterpene lactones [Internet]. Journal of Molecular Structure. 2012 ; 1008 24-28.[citado 2026 maio 09 ] Available from: https://doi.org/10.1016/j.molstruc.2011.11.012 -
Vancouver
Sass DC, Heleno VCG, Soares ACF, Lopes JLC, Constantino MG. Detailed 1H and 13C NMR structural assignment and relative stereochemistry determination for three new and one known semi-synthetic sesquiterpene lactones [Internet]. Journal of Molecular Structure. 2012 ; 1008 24-28.[citado 2026 maio 09 ] Available from: https://doi.org/10.1016/j.molstruc.2011.11.012 - Adição seletiva de hidreto em lactonas sesquiterpênicas
- One-step conversion of a furanoheliangolide into an eremantholide
- One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent
- Detailed assignment of 'ANTPOT.1 H' and 'ANTPOT.13 C' NMR data of diels-alder aducts
- Complete ¹H and ¹³C NMR data assignment for a new furanoheliangolide and an eremntholide obtained by selective reduction of lychnofolide with stryker's reagent
- Complete structural assignment of 'ANTPOT.1 H'and 'ANTPOT.13 C' NMR data for two prepared furanoheliangolides and their products obtained with Stryker's reagent
- Structural assignment of Diel-Alder adducts: an experimental and theoretical approach
- Selectivity in reduction of natural furanoheliangolides with Stryker's reagent
- Spectral assignments and reference data: Total assignment of 'ANTPOT.1 H' and 'ANTPOT. 13 C' NMR data for the sesquiterpene lactone 15-deoxygoyazensolide
- Bloco da quimica organica
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