55 research outputs found
An NMR tool for cyclodextrin selection in enantiomeric resolution by high-performance liquid chromatography.
Complexation-induced chemical shifts and diffusion coefficients (HR-DOSY) of enantiomers with native and derivatized cyclodextrins were used for calculations of the apparent binding constants of three cyclohexanone inclusion complexes. Correlations between these data and high-performance liquid chromatography were established, revealing that this approach can be applied as an alternative method to predict enantiomeric discrimination
Essential oils of seven Brazilian Baccharis: a prospective approach on their ecological role.
A description of the habitat and areas where seven Baccharis species (B.caprarifolia male and female, B.dracunculifolia male and female, B.myriocephala, B. platypoda, B. tridentata, B. vincifolia) occur, is presented. The essential oils of the aerial parts were obtained by hydrodistillation and examined by gas chromatography and gas chromatography/mass spectroscopy. The major constituents were identified by mass spectra comparison with those in the Wiley/NBS library and with thoseof standard commercial, synthetic and isolated compounds. A seasonal and daytime variation in oil composition between female and male plants was observed. The essential oil variation was first correlated to pollination but preliminary field observations showed this to be a complex problem and the floral scent was not easily related to a pollination advertisement or vector
Molecular cloning and functional characterization of a catalase gene from a Bacillus safensis strain isolated from an oil-impacted Brazilian mangrove sediment.
Genome Sequence Of Bacillus Safensis Cfa06, Isolated From Biodegraded Petroleum In Brazil.
Bacillus safensis is a microorganism recognized for its biotechnological and industrial potential due to its interesting enzymatic portfolio. Here, as a means of gathering information about the importance of this species in oil biodegradation, we report a draft genome sequence of a strain isolated from petroleum.
Screening of bacterial isolates from Brazilian oil-impacted mangrove for lipase and esterase activities.
Rational bioprospecting and identi cation of genes from sugarcane endophytic fungi Epicoccum nigrum and Epicoccum sp. involved in the biosynthesis of bioactive metabolites.
Limitations in determining enantiomeric excess of alcohols by 31P-NMR of the phosphonate derivatives
The use of diastereomeric alcohol dialkylphosphonate derivatives to determine the enantiomeric excesses via 31P-NMR signal ratios of anisochronous meso and threo isomers was successfully applied to secondary alcohols (Feringa s method). Expansion of the methodology to primary alcohols possessing the hydroxyl groups thethered to the stereogenic centers by two or more methylene groups proved the method to be inefficent. The comparison between the coupled and decoupled spectra is important in order to identify the signals corresponding to the dialkylphosphonates. Nevertheless the methodology should be applied whenever the amount of the alcohol and its structure are not the limiting factors.O uso de derivados fosfonatos de dialquila diastereoisoméricos na determinação de excessos enantioméricos através da razão entre os sinais de 31P-NMR anisócronos dos isômeros meso e treo, foi bem sucedido para álcoois secundários (método de Feringa), porém revelou-se ineficiente para álcoois primários com dois ou mais grupos metilênicos entre as hidroxilas e os centros estereogênicos. Observou-se adicicionalmente que era importante obter os espectros acoplados e desacoplados para se certificar dos picos correspondentes aos fosfonatos de dialquila. Entretanto, esta metodologia merece ser aplicada sempre que a quantidade de álcool disponível e sua estrutura não forem fatores limitantes.293298Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES
Synthesis of rearranged unsaturated drimane derivatives
A full account to the preparation and application of three appropriately substituted vinylcyclohexenes (2,2-dimethyl-3-vinylcyclohex-3-en-1-ol, 2,2-dimethyl-3-vinylcyclohex-3-en-1-one and 3,3-dimethyl-2-vinylcyclohexene) in thermal Diels-Alder reactions with alpha,beta-unsaturated esters (methyl tiglate and methyl angelate) is given. This approach delivered the racemic synthesis of ten octalin derivatives bearing a rearranged drimane skeleton (4 diastereomers of 1-methoxycarbonyl-6-hydroxy-1,2,5,5-tetramethyl-1,2,3,5,6,7, 8,8a-octahydronaphthalene; 1-methoxycarbonyl-6-oxo-1,2,5,5-tetramethyl-1,2,3,4,5,6,7,8-octahydronaphthalene; 2-methoxycarbonyl-6-oxo-1,2,5,5-tetramethyl-1,2,3,5,6,7,8,8a-octahydronaphthalene; 3 diastereomers of 1-methoxycarbonyl-1,2,5,5-tetramethyl-1,2,3,5,6,7,8,8a-octahydronaphthalene and 2-methoxycarbonyl-1,2,5,5-tetramethyl-1,2,3,5,6,7,8,8a-octahydronaphthalene) . Central synthetic features included preparation of enoltriflates by Stang's protocol and the successful palladium-catalyzed cross-coupling reaction (Stille reaction) of the triflate with the tri-n-butylvinylstannane. The octalins relative stereochemistry was unequivocally ascertained by spectroscopic methods and/or X-ray crystallography and these data now stand as useful tools to support the correct assignment of related natural products usually isolated in minute amounts.O presente trabalho relata a preparação e aplicação de três vinilcicloexenos devidamente funcionalizados (2,2-dimetil-3-vinilcicloex-3-en-1-ol, 2,2-dimetil-3-vinilcicloex-3-en-1-ona e 3,3-dimetil-2-vinilcicloexeno) em reações de Diels-Alder com ésteres a,b-insaturados (tiglato de metila e angelato de metila). Esta abordagem levou à síntese racêmica de dez octalinas possuindo esqueleto drimânico rearranjado (4 diastereoisômeros do 1-metoxicarbonil-6-hidroxi-1,2,5,5-tetrametil-1,2,3,5,6,7,8,8a-octaidronaftaleno; 1-metoxicarbonil-6-oxo-1,2,5,5-tetrametil-1,2,3,4,5,6,7,8 -ocataidronaftaleno; 2-metoxicarbonil-6-oxo-1,2,5,5-tetrametil-1,2,3,5,6,7, 8,8a-octaidronaftaleno; 3 diastereoisômeros do 1-metoxicarbonil-1,2,5,5-tetrametil-1,2,3,5,6,7,8,8a-octaidronaftaleno e 2-metoxicarbonil-1,2,5,5-tetrametil-1,2,3,5,6,7,8,8a-octaidronaftaleno) . Para a preparação dos dienos, utilizou-se a reação de acoplamento catalisada por paládio (reação de Stille) entre enoltriflatos (preparados pelo protocolo de Stang) e tri-n-butilvinilestanana. A estereoquímica relativa dos produtos foi estabelecida a partir de métodos espectroscópicos e análise de difração de raios-X de alguns dos derivados. Estes dados podem servir para a identificação de novos produtos naturais e corrigir algumas estruturas da literatura.391402Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq
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