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Progressive-convergent elucidation of stereochemistry in complex polyols. The absolute configuration of (-)-sagittamide ALIEVENS, Sarah C; MOLINSKI, Tadeusz F.Journal of the American Chemical Society. 2006, Vol 128, Num 36, pp 11764-11765, issn 0002-7863, 2 p.Article

(8R)- and (8-S)-hepoxilin A3. Assignment of configuration and conversion to biologically active conjugates with glutathioneCOREY, E. J; WEI-GUO SU.Tetrahedron letters. 1990, Vol 31, Num 15, pp 2113-2116, issn 0040-4039Article

Prokaryotic triterpenois. (22r.32r)-34,35-dinorbacteriohopane-32,33-diols from Acetobacter aceti ssp. sylinum : new bacteriohopane derivateives with shortened side-chainPEISELER, B; ROHMER, M.Journal of the Chemical Society. Perkin transactions. I. 1991, Num 10, pp 2449-2453, issn 0300-922XArticle

The CIP sequence rules : analysis and proposal for a revisionMATA, P; LOBO, A. M; MARSHALL, C et al.Tetrahedron : asymmetry (Print). 1993, Vol 4, Num 4, pp 657-668, issn 0957-4166Article

Determining the absolute configuration of hindered secondary alcohols - a modified Horeau' methodBARNEKOW, D. E; CARDELLINA, J. H.Tetrahedron letters. 1989, Vol 30, Num 28, pp 3629-3632, issn 0040-4039, 4 p.Article

Chiral azophenolic acerands: color indicators to judge the absolute configuration of chiral aminesKANEDA, T; HIROSE, K; MISUMI, S et al.Journal of the American Chemical Society. 1989, Vol 111, Num 2, pp 742-743, issn 0002-7863, 2 p.Article

Poststatin, a new inhibitor of prolyl endopeptidase. III. Optical resolution of 3-amino-2-hydroxyvaleric acid and absolute configuration of poststatinTSUDA, M; MURAOKA, Y; NAGAI, M et al.Journal of antibiotics (Tokyo. 1968). 1996, Vol 49, Num 3, pp 281-286, issn 0021-8820Article

From recreational mathematics to molecular designMISLOW, K.Bulletin de la Société chimique de France. 1994, Vol 131, Num 5, pp 534-538, issn 0037-8968Article

Halogen-Bonding Interaction Stabilizing Cluster-type Diastereomeric Salt CrystalsKOBAYASHI, Yuka; MAEDA, Jin; ANDO, Tetsuo et al.Crystal growth & design. 2010, Vol 10, Num 2, pp 685-690, issn 1528-7483, 6 p.Article

Confirmation of the absolute configuration of dolichantoside and isodolichantoside by synthesis from (-)-secologaninACHENBACH, H; BENIRSCHKE, M.Phytochemistry. 1997, Vol 44, Num 7, pp 1387-1390, issn 0031-9422Article

The absolute configuration of (+)-1,2,4,5,6-penta-O-benzyl-myo-inositolANEJA, R; ANEJA, S; PATHAK, V. P et al.Tetrahedron letters. 1994, Vol 35, Num 33, issn 0040-4039, 5964, 6061-6062 [3 p.]Article

Diastereoselective addition of organometallic reagents to chiral imines and 1,3-oxazolidinesHIGASHIYAMA, K; INOUE, H; TAKAHASHI, H et al.Tetrahedron letters. 1992, Vol 33, Num 2, pp 235-238, issn 0040-4039Article

Muricatacin : a simple biologically active acetogenin derivative from the seeds of Annona muricata (annonaceae)RIESER, M. J; KOZLOWSKI, J. F; WOOD, K. V et al.Tetrahedron letters. 1991, Vol 32, Num 9, pp 1137-1140, issn 0040-4039, 4 p.Article

Microscale CD method for determining absolute configurations of acyclic amino tetrols and amino pentols. Structures of aminobacteriohopanepolyols from the methylotrophic bacterium Methylococcus luteusPENG ZHOU; BEROVA, N; NAKANISHI, K et al.Journal of the American Chemical Society. 1991, Vol 113, Num 10, pp 4040-4042, issn 0002-7863Article

Efficient preparation of (R)-(-)-cryptone from (+)-nopinone and its transformation into noroxopenlanfuranKATO, M; WATANABE, M; VOGLER, B et al.Journal of the Chemical Society. Chemical communications. 1990, Num 23, pp 1706-1707, issn 0022-4936, 2 p.Article

The absolute configuration and synthesis of natural (-)-dolastatin 10PETTIT, G. R; SHEO BUX SINGH; HOGAN, F et al.Journal of the American Chemical Society. 1989, Vol 111, Num 14, pp 5463-5465, issn 0002-7863Article

Grimaldone, a tricyclic sesquiterpenoid from Mannia fragrans. Crystal structure analysisHUNECK, S; CONNOLLY, J. D; FREER, A. A et al.Phytochemistry. 1988, Vol 27, Num 5, pp 1405-1407, issn 0031-9422Article

Stereochemical studies of polyols from the polyene macrolide lienomycinPAWLAK, J; NAKANISHI, K; IWASHITA, T et al.Journal of organic chemistry. 1987, Vol 52, Num 13, pp 2896-2901, issn 0022-3263Article

Absolute configurations of rehmaionosides A, B, and C and rehmapicroside three new ionone glucosides and a new monoterpene glucoside from rehmanniae radixYOSHIKAWA, M; FUKUDA, Y; TANIYAMA, T et al.Chemical and pharmaceutical bulletin. 1986, Vol 34, Num 5, pp 2294-2297, issn 0009-2363Article

Direkte Bestimmung der absoluten Konfiguration chiraler Alkylgluconamide durch Benetzbarkeitsmessungen = Direct assignment of absolute configuration of chiral alkyl gluconamides by wettability measurementsWANG, J.-L; LAHAV, M; LEISEROWITZ, L et al.Angewandte Chemie. 1991, Vol 103, Num 6, pp 698-699, issn 0044-8249Article

Antineoplastic agents. CCXX, Synthesis of natural (-)-dolastatin 151PETTIT, G. R; HERALD, D. L; SHEO BUX SINGH et al.Journal of the American Chemical Society. 1991, Vol 113, Num 17, pp 6692-6693, issn 0002-7863Article

Elucidation of the absolute configurations of amino acids and amines by the modified Mosher's methodKUSUMI, T; FUKUSHIMA, T; OHTANI, I et al.Tetrahedron letters. 1991, Vol 32, Num 25, pp 2939-2942, issn 0040-4039Article

Secondary mould metabolites. XXXIV, Isolation and structure elucidation of illudosin, a novel sesquiterpene from Clitocybe illudens using one and two dimensional NMR techniquesARNONE, A; CARDILLO, R; NASINI, G et al.Journal of the Chemical Society. Perkin transactions. I. 1991, Num 8, pp 1787-1791, issn 0300-922XArticle

The absolute configuration of ketamine : a general anaesthetic. The crystal structure of teh (R,R)-tartrate salt of (-)-(S)-ketamineRATTI-MOBERG, E; GROTH, P; AASEN, J et al.Acta chemica scandinavica (Copenhagen. 1989). 1991, Vol 45, Num 1, pp 108-110, issn 0904-213XArticle

Absolute Konfiguration und enantiomere Reinheit von Celiprolol = Configuration absolue et pureté énantiomérique au céliprolol = Absolute configuration and enantiomeric purity of CeliprololHOFER, O; SCHLÖGL, K.Arzneimittel-Forschung. 1986, Vol 36, Num 8, pp 1157-1161, issn 0004-4172Article

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