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Results 1 to 25 of 19406

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Cleavage reaction of 5β,6β steroidal epoxides carrying different groups at C-3TEME CENTURION, O. M; GALAGOVSKY, L. R; GROS, E. G et al.Steroids. 1995, Vol 60, Num 7, pp 434-438, issn 0039-128XArticle

USE OF N-LITHIOETHYLENEDIAMINE IN THE DOUBLE BOND ISOMERIZATION AND DEGRADATION OF STEROL SIDE CHAINSAYANOGLU E; CHAN A; DJERASSI C et al.1979; TETRAHEDRON; GBR; DA. 1979; VOL. 35; NO 13; PP. 1591-1594; BIBL. 17 REF.Article

INFLUENCE DE L'INSATURATION DELTA 20 (22) SUR LA FRAGMENTATION DU CYCLE D DES STEROIDES.SCHMIT JP; CHARETTE JJ.1977; ORG. MASS SPECTROM.; G.B.; DA. 1977; VOL. 12; NO 8; PP. 488-492; ABS. ANGL.; BIBL. 5 REF.Article

Fern constituents : triterpenoids isolated from Polypodium vulgare, P. fauriei and P. virginianumARAI, Y; YAMAIDE, M; YAMAZAKI, S et al.Phytochemistry. 1991, Vol 30, Num 10, pp 3369-3377, issn 0031-9422Article

STEREOSPECIFIC SYNTHESIS OF THE FOUR 20,22-EPOXYCHOLESTEROLS AND OF (Z)-20(22)-DEHYDROCHOLESTEROL.CHANG YON BYON; GUT M.1976; J. ORG. CHEM.; U.S.A.; DA. 1976; VOL. 41; NO 23; PP. 3716-3722; BIBL. 27 REF.Article

SYNTHESES DE TRITERPENES POTENTIELLEMENT ANTI-CANCEREUXDE REINACH HIRTZBACH F.1973; AO-CNRS-10528; FR.; DA. 1973; PP. 1-132; BIBL. 6 P. 1/2; (THESE DOCT. SCI. PHYS.; LOUIS PASTEUR STRASBOURG)Thesis

Double bond migration on the 22(17→28) abeo-lupane skeletonFUCHINO, H; NOZAWA, O; TANAKA, N et al.Chemical and pharmaceutical bulletin. 1994, Vol 42, Num 9, pp 1745-1749, issn 0009-2363Article

Ene approach for concurrent control over the chiral centres at C-20 and C-22 of steroid side chains: a highly stereocontrolled synthesis of (20S,22R)-(erythro-)22-hydroxy-23,24-acetylenic steroid side chainsMIKAMI, K; LOH, T.-P; NAKAI, T et al.Journal of the Chemical Society. Chemical communications. 1988, Num 21, pp 1430-1431, issn 0022-4936Article

SELECTIVITY IN THE HYDROGENATION OF 20(22)-DEHYDROSTEROIDSDUBOIS GE.1982; J. ORG. CHEM.; ISSN 0022-3263; USA; DA. 1982; VOL. 47; NO 25; PP. 5035-5037; BIBL. 21 REF.Article

Conversion of lupeol into dammarane derivativesOHTA, S; TORI, M; TSUYUKI, T et al.Bulletin of the Chemical Society of Japan. 1983, Vol 56, Num 7, pp 2187-2188, issn 0009-2673Article

Oygenated sterols as inhibitors of enzymatic conversion of dihydrolanosterol into cholesterolSATO, Y; SONODA, Y; MORISAKI, M et al.Chemical and pharmaceutical bulletin. 1984, Vol 32, Num 8, pp 3305-3308, issn 0009-2363Article

THE STEREOCHEMISTRY OF STEROLS AT C-20 AND ITS BIOSYNTHETIC IMPLICATION.NES WR; VARKEY TE; KREVITZ K et al.1977; J. AMER. CHEM. SOC.; U.S.A.; DA. 1977; VOL. 99; NO 1; PP. 260-262; BIBL. 18 REF.Article

APPLICATION OF THE WITTIG REACTION TO THE SYNTHESIS OF STEROIDAL SIDE CHAINS. POSSIBILITY OF 3BETA -PHENOXY FORMATION AS A SECONDARY REACTIONSCHMIT JP; PIRAUX M; PILETTE JF et al.1975; J. ORG. CHEM.; U.S.A.; DA. 1975; VOL. 40; NO 11; PP. 1586-1588; BIBL. 11 REF.Article

Application of [2,3]Wittig rearrangement in steroid side chain synthesis: a new entry to (22R)-hydroxy-23-acetylenic side chains via the β-face rearrangementMIKAMI, K; KAWAMOTO, K; NAKAI, T et al.Chemistry Letters. 1985, Num 11, pp 1719-1722, issn 0366-7022Article

Preparation and absolute configuration at C(22) of 21,26,27-trinor-5α-cholestane-22,25-diol derivativesPOUZAR, V; VASICKOVA, S; DRASAR, P et al.Collection of Czechoslovak chemical communications. 1983, Vol 48, Num 8, pp 2423-2435, issn 0010-0765Article

Stereospecific syntheses of the four epimers of 7,22-dihydroxycholesterolAMANN, A; OURISSON, G; BANG LUU et al.Synthesis (Stuttgart). 1987, Num 11, pp 1002-1005, issn 0039-7881Article

Lactol-ene reactions : an efficient access to the synthesis of 22R, 25-dihydroxy steroid side chainsMIKAMI, K; KISHINO, H; MATSUEDA, H et al.Synlett. 1993, Num 7, pp 497-498, issn 0936-5214Article

Two novel secoergosterols from the fungus Tylopilus plumbeoviolaceusWU, S.-H; LUO, X.-D; MA, Y.-B et al.Journal of natural products (Print). 2000, Vol 63, Num 4, pp 534-536, issn 0163-3864Article

IL-22 : A critical mediator in mucosal host defenseAUJLA, S. J; KOLLS, J. K.Journal of molecular medicine (Berlin. Print). 2009, Vol 87, Num 5, pp 451-454, issn 0946-2716, 4 p.Article

Application of [2,3]Wittig and [3,3]Claisen rearrangements in steroid side chain synthesis. A highly stereocontrolled entry to either (22S)- or (22R)-hydroxy-23-carboxylic acidMIKAMI, K; KAWAMOTO, K; NAKAI, T et al.Tetrahedron letters. 1986, Vol 27, Num 40, pp 4899-4902, issn 0040-4039Article

STEREOCHEMISTRY OF 14,22-ETHERS FORMED BY CYCLIZATION OF DELTA 7-22-HYDROXY STEROIDSABERHART DJ; CASPI E; WEEKS CM et al.1979; J. ORG. CHEM.; USA; DA. 1979; VOL. 44; NO 1; PP. 75-77; BIBL. 6 REF.Article

Short-step steroselective synthesis of 2α, 3α, 22-triacetoxy-23,24-dinor-5α-cholan-6-one : key intermediate for the preparation of 24-norbrassinolide, dilicholide and dolichosteroneHAZRA, B. G; PORE, V. S; JOSHI, P. L et al.Journal of the Chemical Society. Perkin transactions. I. 1993, Num 15, pp 1819-1822, issn 0300-922XArticle

Welche Kältemittel in der Zukunft? = Which refrigerant in the future?DOÊRING, R.Die Kälte und Klimatechnik. 1990, Vol 43, Num 9, pp 472-482, issn 0343-2246, 6 p.Article

Th17 cytokines and mucosal immunityDUBIN, Patricia J; KOLLS, Jay K.Immunological reviews. 2008, Vol 226, pp 160-171, issn 0105-2896, 12 p.Article

IL-22, but Not IL-17, Dominant Environment in Cutaneous T-cell LymphomaMIYAGAKI, Tomomitsu; SUGAYA, Makoto; SUGA, Hiraku et al.Clinical cancer research (Print). 2011, Vol 17, Num 24, pp 7529-7538, issn 1078-0432, 10 p.Article

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