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Results 1 to 25 of 16340

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The Chemistry and Biology of Nakiterpiosin ― C-nor-D-HomosteroidsSHUANHU GAO; QIAOLING WANG; GELIN WANG et al.Synlett (Stuttgart). 2012, Num 16, pp 2298-2310, issn 0936-5214, 13 p.Article

Bismuth(III) Triflate-Catalyzed Direct Conversion of Corticosteroids into Highly Functionalized 17-Ketosteroids by Cleavage of the C17-Dihydroxyacetone Side ChainPINTO, Rui M. A; SALVADOR, Jorge A. R; LE ROUX, Christophe et al.Journal of organic chemistry. 2009, Vol 74, Num 21, pp 8488-8491, issn 0022-3263, 4 p.Article

Ruthenium-catalyzed mild C-H oxyfunctionalization of cyclic steroidal ethersJONG SEOK LEE; HUI CAO; FUCHS, Philip L et al.Journal of organic chemistry. 2007, Vol 72, Num 15, pp 5820-5823, issn 0022-3263, 4 p.Article

First synthesis of free cholesterol-BODIPY conjugatesZAIGUO LI; MINTZER, Evan; BITTMAN, Robert et al.Journal of organic chemistry. 2006, Vol 71, Num 4, pp 1718-1721, issn 0022-3263, 4 p.Article

Direct electrospray tandem mass spectrometry of the unstable hydroperoxy bishemiacetal product derived from cholesterol ozonolysisPULFER, Melissa K; HARRISON, Kathleen; MURPHY, Robert C et al.Journal of the American Society for Mass Spectrometry. 2004, Vol 15, Num 2, pp 194-202, issn 1044-0305, 9 p.Article

Total synthesis of methyl protodioscin: A potent agent with antitumor activityCHENG, Mao S; WANG, Qian L; QUAN TIAN et al.Journal of organic chemistry. 2003, Vol 68, Num 9, pp 3658-3662, issn 0022-3263, 5 p.Article

Concomitant C-ring expansion and D-ring formation in lanosterol biosynthesis from squalene without violation of Markovnikov's ruleHESS, B. Andes.Journal of the American Chemical Society. 2002, Vol 124, Num 35, pp 10286-10287, issn 0002-7863, 2 p.Article

[3,3]-Claisen rearrangements in 24α-methyl steroid synthesis application to campesterol, crinosterol, and Δ25-crinosterol side chain constructionKHRIPACH, Vladimir A; ZHABINSKII, Vladimir N; KONSTANTINOVA, Olga V et al.Steroids. 2002, Vol 67, Num 7, pp 597-603, issn 0039-128XArticle

26-Nor-25-isopropyl-ergosta-5,7,22E-trien-3β-ol: a new C29 sterol from the sponge Agelas sceptrum from JamaicaHU, Jin-Feng; KELLY, Michelle; HAMANN, Mark T et al.Steroids. 2002, Vol 67, Num 9, pp 743-747, issn 0039-128X, 5 p.Article

An efficient route for the preparation of a 21-fluoro progestin-16α, 17α-dioxolane, a high-affinity ligand for PET imaging of the progesterone receptorVIJAYKUMAR, Dange; WANG MAO; KIRSCHBAUM, Karen S et al.Journal of organic chemistry. 2002, Vol 67, Num 14, pp 4904-4910, issn 0022-3263, 7 p.Article

Corticosteroid decomposition via a mixed anhydrideCONROW, Raymond E; DILLOW, Glen W; LIANGQIAO BIAN et al.Journal of organic chemistry. 2002, Vol 67, Num 19, pp 6835-6836, issn 0022-3263, 2 p.Article

Efficient synthesis of IPL576,092: A novel anti-asthma agentYAPING SHEN; BURGOYNE, David L.Journal of organic chemistry. 2002, Vol 67, Num 11, pp 3908-3910, issn 0022-3263, 3 p.Article

Microwave-assisted Stille-coupling of steroidal substratesSKODA-FÖLDES, Rita; PFEIFFER, Péter; HORVATH, Judit et al.Steroids. 2002, Vol 67, Num 8, pp 709-713, issn 0039-128X, 5 p.Article

Synthesis of (25R)-26-hydroxycholesterolWILLIAMS, John R; DEPING CHAI; WRIGHT, Dominic et al.Steroids. 2002, Vol 67, Num 13-14, pp 1041-1044, issn 0039-128X, 4 p.Article

Total synthesis of ent-cholesterol via a steroid C, D-ring side-chain synthonXIN JIANG; COVEY, Douglas F.Journal of organic chemistry. 2002, Vol 67, Num 14, pp 4893-4900, issn 0022-3263, 8 p.Article

Synthesis of 3-epi-6,7-dideoxyxestobergsterol AKAJI, Yuko; KOAMI, Takeshi; NAKAMURA, Atsuko et al.Chemical and pharmaceutical bulletin. 2000, Vol 48, Num 10, pp 1480-1483, issn 0009-2363Article

SYNTHESE TOTALE DE 11-HETERO STEROÏDES = TOTAL SYNTHESIS OF 11-HETERO STEROIDSCachoux, Frédéric; Santelli, Maurice.2000, 300 p.Thesis

An improved synthesis of (20R, 22R)-cholest-5-ene-3β, 20,22-triol, an intermediate in steroid hormone formation and an activator of nuclear orphan receptor LXRαBENFANG RUAN; WILSON, W. K; SCHROEPFER, G. J et al.Steroids. 1999, Vol 64, Num 6, pp 385-395, issn 0039-128XArticle

O-(fluoresceinylmethyl)hydroxylamine (OFMHA) : A reagent for the preparation of fluorescent O-(fluoresceinylmethyl)oxime (FMO)-steroid conjugatesADAMCZYK, M; CHEN, Y.-Y; GROTE, J et al.Steroids. 1999, Vol 64, Num 4, pp 283-290, issn 0039-128XArticle

Study on steroidal oximinoethers : Synthesis and stereostructure by NMR spectroscopySOHAR, P; BODOR, A; SCHWARTZ, R et al.Steroids. 1999, Vol 64, Num 4, pp 246-251, issn 0039-128XArticle

Reaction of androst-5-en-17-one with hypobromous acid and its use for synthesis of 19-oxygenated 5-ene and 4-en-6-one steroidsNUMAZAWA, M; YAMADA, K.Steroids. 1998, Vol 63, Num 2, pp 62-69, issn 0039-128XArticle

Synthesis of tritium-labelled biologically active analogues of progesterone by selective hydrogenation of 16α, 17α-cyclohex-3'-en-pregna-1,4-dien-3,20-dioneSHEVCHENKO, V. P; NAGAEV, I. Yu; POTAPOVA, A. V et al.Journal of labelled compounds & radiopharmaceuticals. 1998, Vol 41, Num 10, pp 919-925, issn 0362-4803Article

An alternative synthesis of 4,4-dimethyl-5α-cholesta-8,14,24-trien-3β-ol, an intermediate in sterol biosynthesis and a reported activator of meiosis and of nuclear orphan receptor LXRαRUAN, B; WILSON, W. K; SCHROEPFER, G. J et al.Bioorganic & medicinal chemistry letters (Print). 1998, Vol 8, Num 3, pp 233-236, issn 0960-894XArticle

The synthesis of taurine-conjugated bile acids and bile acid sulfates labeled with 14C or 3H in the taurine moietyZHANG, J; GRIFFITHS, W. J; SJÖVALL, J et al.Journal of labelled compounds & radiopharmaceuticals. 1997, Vol 39, Num 2, pp 159-164, issn 0362-4803Article

Convergent synthesis of 1α,25-dihydroxy-2β-(3-hydroxypropoxy)vitamin D3 (ED-71)HATAKEYAMA, S; IKEDA, T; MAEYAMA, J et al.Bioorganic & medicinal chemistry letters (Print). 1997, Vol 7, Num 22, pp 2871-2874, issn 0960-894XArticle

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