Zobrazeno 1 - 10
of 1 047
pro vyhledávání: '"R A Pascal, Jr"'
Publikováno v:
European Journal of Organic Chemistry. 11/8/2018, Vol. 2018 Issue 41, p5706-5710. 5p.
Publikováno v:
Chemistry - A European Journal. 3/2/2018, Vol. 24 Issue 13, p3113-3116. 4p.
Autor:
Xiao, Yonglong1 (AUTHOR), Mague, Joel T.1 (AUTHOR), Donahue, James P.1 (AUTHOR), Wilson, Laura J.2 (AUTHOR), Kraml, Christina M.2 (AUTHOR), Pascal, Robert A.1 (AUTHOR) rpascal@tulane.edu
Publikováno v:
Chemistry - A European Journal. 7/8/2020, Vol. 26 Issue 38, p8458-8464. 7p.
Autor:
Du, Yuchen1 (AUTHOR), McSkimming, Alex1 (AUTHOR), Mague, Joel T.1 (AUTHOR), Pascal, Robert A.1 (AUTHOR) rpascal@tulane.edu
Publikováno v:
Chemistry - A European Journal. 7/20/2022, Vol. 28 Issue 41, p1-10. 10p.
Publikováno v:
Journal of Lipid Research, Vol 22, Iss 1, Pp 171-177 (1981)
A relatively simple method is described for the isolation of zymosterol (5 alpha-cholesta-8, 24-dien-3 beta-ol) of high purity from baker's yeast. Also presented are detailed spectral properties, including 13C NMR spectral analyses, of zymosterol and
Externí odkaz:
https://doaj.org/article/195d3cd873874759b83fc0c214ce8be6
Publikováno v:
Journal of Lipid Research, Vol 21, Iss 5, Pp 571-584 (1980)
The chemical syntheses of a number of 14 alpha-hydroxymethyl sterols and 14 alpha -hydroxymethyl-15 alpha-hydroxysterols and their derivatives have been pursued to permit evaluation of their activity in the inhibition of sterol biosynthesis in animal
Externí odkaz:
https://doaj.org/article/69a07bfef8804ffbbb5fac6c0427ece8
Autor:
R A Pascal, Jr, G J Schroepfer, Jr
Publikováno v:
Journal of Lipid Research, Vol 21, Iss 1, Pp 118-122 (1980)
Reported herein is the chemical synthesis of 5 alpha-cholest-7-en-3 beta, 14 alpha-diol by mild Wolff-Kishner reduction of 3 beta-acetoxy-8 alpha, 14 alpha-epoxy-5 alpha-cholestan-7-one. The preparation of 5 alpha-cholest-7-en-14 alpha-ol-3-one from
Externí odkaz:
https://doaj.org/article/834f1820ec534308817572a4fa1abee2
Publikováno v:
Journal of Lipid Research, Vol 20, Iss 5, Pp 570-578 (1979)
Reported herein are chemical syntheses of 14 alpha-hydroxymethyl-5 alpha-cholest-8-en-3 beta-ol, 14 alpha-hydroxymethyl-5 alph-cholest-7-en-3 beta-ol, and 14 alpha-hydroxymethyl-5 alpha-cholest-6-en 3 beta-ol. These compounds were obtained in pure fo
Externí odkaz:
https://doaj.org/article/1170a9bcfd68492198d50b258029d54a
Publikováno v:
Journal of Lipid Research, Vol 29, Iss 11, Pp 1543-1548 (1988)
Short syntheses of 24-thia-5 alpha,20 xi-cholestan-3 beta-ol, 24-methyl-24-aza-5 alpha,20 xi-cholestan-3 beta-ol, and 24-nor-5 alpha,20 xi-cholan-3 beta-ol from 3 beta-hydroxy-5 alpha-pregnan-20-one are described. The products and synthetic intermedi
Externí odkaz:
https://doaj.org/article/6b466637e694445e8816bc737584433b
Autor:
R A Pascal, Jr, D L Ziering
Publikováno v:
Journal of Lipid Research, Vol 27, Iss 2, Pp 221-224 (1986)
We report herein the syntheses of several analogues of stearic acid in which oxygen or sulfur atoms or sulfoxide groups have replaced the methylene groups at either position 9 or position 10 of the polymethylene chains. These compounds have been full
Externí odkaz:
https://doaj.org/article/d25b0c2d7fc043c5b2f043c0668f88d9