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Comprehensive Analysis of Phenolic Compounds in <i>Solanum glaucophyllum</i> Desf. [PDF]
Heymann T, Autzen S, Glomb MA.
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Molecular and isotopic archaeology: Top grade tools to investigate organic archaeological materials [PDF]
Armelle Charrié-Duhaut +4 more
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Sterol 14-alpha demethylase (CYP51) activity in Leishmania donovani is likely dependent upon cytochrome P450 reductase 1. [PDF]
Tulloch LB +9 more
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Rational design of cholesterol oxidase for efficient bioresolution of cholestane skeleton substrates. [PDF]
Qin HM +9 more
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A survey of marine natural compounds and their derivatives with anti-cancer activity reported in 2010. [PDF]
Schumacher M +3 more
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Naturally Occurring Norsteroids and Their Design and Pharmaceutical Application. [PDF]
Dembitsky VM.
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Tetrahedron, 1971
Abstract 2-oxa ( 11 ), 2-thia ( 12 ) and 2-aza ( 19 ), 5α-cholestanes were prepared from the sulfonic esters of A-seco-2-nor-5α-cholestan-1,3-diol ( 9 and 10 ). Although cyclopentamethylenediphenylphosphonium tosylate ( 4 ) could be obtained from pentan-α,ω-ditosyloxy ( 6 ) and Ph 2 PK, attempts to prepare 3-phosphacholestane ( 16 ) in a similar ...
Y. Kashman, E.D. Kaufman
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Abstract 2-oxa ( 11 ), 2-thia ( 12 ) and 2-aza ( 19 ), 5α-cholestanes were prepared from the sulfonic esters of A-seco-2-nor-5α-cholestan-1,3-diol ( 9 and 10 ). Although cyclopentamethylenediphenylphosphonium tosylate ( 4 ) could be obtained from pentan-α,ω-ditosyloxy ( 6 ) and Ph 2 PK, attempts to prepare 3-phosphacholestane ( 16 ) in a similar ...
Y. Kashman, E.D. Kaufman
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Acta Crystallographica Section C Crystal Structure Communications, 1996
The crystal structure of the title compound, naphtho[2,3-b]cholestane, C 35 H 50 , is composed of independent molecules with normal molecular dimensions and no unusual contacts shorter than van der Waals distances.
M. Parvez +3 more
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The crystal structure of the title compound, naphtho[2,3-b]cholestane, C 35 H 50 , is composed of independent molecules with normal molecular dimensions and no unusual contacts shorter than van der Waals distances.
M. Parvez +3 more
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Hofmann degradation of 5α-cholestan-4α- and 5α-cholestan-4β-yltrimethylammonium salts
J. Chem. Soc. B, 1970Alkaline degradation of 5α-cholestan-4α-yltrimethylammonium iodide gives mainly 5α-cholestan-4α-yldimethyl-amine with a little cholest-3-ene, while the 4β-isomer gives cholest-4-ene. The unstable 4β-iodide also readily yields cholest-4-ene in boiling neutral alcohol.
E. N. Wall, J. McKenna
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