Literature DB >> 1270711

A stereoselective synthesis of the 24(R),25-dihydroxycholesterol side chain.

J J Partridge, V Toome, M R Uskokovic.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1976        PMID: 1270711     DOI: 10.1021/ja00428a076

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


× No keyword cloud information.
  4 in total

1.  A fast and simplein situ method for the determination of the absolute configuration of amino acid esters using the chiroptical properties of their Eu(FOD)3 complexes.

Authors:  V Toome; B Wegrzynski
Journal:  Amino Acids       Date:  1992-06       Impact factor: 3.520

2.  Anomalous enantioselectivity in the sharpless asymmetric dihydroxylation reaction of 24-nor-5beta-cholest-23-ene-3alpha,7alpha,12alpha-triol: synthesis of substrates for studies of cholesterol side-chain oxidation.

Authors:  N H Ertel; B Dayal; K Rao; G Salen
Journal:  Lipids       Date:  1999-04       Impact factor: 1.880

3.  Production of C-24- and C-23-oxidized metabolites of 1,25-dihydroxycholecalciferol by cultured kidney cells (LLC PK1) and their presence in kidney in vivo.

Authors:  J L Napoli; C A Martin
Journal:  Biochem J       Date:  1984-05-01       Impact factor: 3.857

4.  (23S)-1,23,25-Trihydroxycholecalciferol, an intestinal metabolite of 1,25-dihydroxycholecalciferol.

Authors:  J L Napoli; R L Horst
Journal:  Biochem J       Date:  1983-07-15       Impact factor: 3.857

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.