One-step conversion of a furanoheliangolide into an eremantholide (2008)
- Authors:
- USP affiliated authors: LOPES, JOAO LUIS CALLEGARI - FCFRP ; CONSTANTINO, MAURICIO GOMES - FFCLRP
- Unidades: FCFRP; FFCLRP
- Subjects: PRODUTOS NATURAIS; SÍNTESE QUÍMICA; FÍSICO-QUÍMICA
- Language: Inglês
- Imprenta:
- Publisher place: Porto de Galinhas
- Date published: 2008
- Conference titles: Brazilian Symposium on Medicinal Chemistry
-
ABNT
SASS, D. C. et al. One-step conversion of a furanoheliangolide into an eremantholide. 2008, Anais.. Porto de Galinhas: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, 2008. . Acesso em: 25 maio 2024. -
APA
Sass, D. C., Heleno, V. C. G., Lopes, J. L. C., & Constantino, M. G. (2008). One-step conversion of a furanoheliangolide into an eremantholide. In . Porto de Galinhas: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. -
NLM
Sass DC, Heleno VCG, Lopes JLC, Constantino MG. One-step conversion of a furanoheliangolide into an eremantholide. 2008 ;[citado 2024 maio 25 ] -
Vancouver
Sass DC, Heleno VCG, Lopes JLC, Constantino MG. One-step conversion of a furanoheliangolide into an eremantholide. 2008 ;[citado 2024 maio 25 ] - Detailed 1H and 13C NMR structural assignment and relative stereochemistry determination for three new and one known semi-synthetic sesquiterpene lactones
- Complete ¹H and ¹³C NMR data assignment for a new furanoheliangolide and an eremntholide obtained by selective reduction of lychnofolide with stryker's reagent
- Detailed assignment of 'ANTPOT.1 H' and 'ANTPOT.13 C' NMR data of diels-alder aducts
- 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
- One-step biomimetic conversion of a furanoheliangolide into an eremantholide using Stryker's reagent
- Adição seletiva de hidreto em lactonas sesquiterpênicas
- Spectral assignments and reference data: Total assignment of 'ANTPOT.1 H' and 'ANTPOT. 13 C' NMR data for the sesquiterpene lactone 15-deoxygoyazensolide
- Structural assignment of Diel-Alder adducts: an experimental and theoretical approach
- Selectivity in reduction of natural furanoheliangolides with Stryker's reagent
- Estudos sobre a síntese de furanoeliangolidos pela reação de Diels-Alder
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