Further studies on the oxy-functionalization of cholesteryl acetate with tert-butyl hydroperoxide and tris(acetylacetonato)iron(III)

DOI: 10.1248/cpb.29.1862

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1862 - 1869 (1981)

Update date:2022-08-03

Topics:

Authors:

Kimura Kimura

Muto Muto

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1248/cpb.29.1862

Full text of DOI:10.1248/cpb.29.1862

NII-Electronic Library Service

Products guided by the article

Product name:cholest-5-ene-3β,7-diol 3-monoacetate

Cas No:77059-25-7

R&D Labs maybe for 77059-25-7

Maithili Life Sciences

Contact:+91 9963263336

Address:Plot#146A, IDA Mallapur, Hyderabad - 500072
Hebei Tianxiang Biological & Pharmaceutical Co., Ltd

Contact:86-0312-6615158

Address:No 42 fazhan street qingyuan county
Li's chemicals

Contact:+86-15850770348

Address:51 OF XIANGFANGCUN ROAD, Nanjing 210002, China
Jinan Aery Pharmaceutical Co,.Ltd

Contact:+8653181263406

Address:1-1916,Building1 Fenghuang SOHO,Fenghuang Road,High-tech Zone,Jinan,Shandong
Nanjing Qirui Material Co., Ltd.

Contact:+86-25-52320053

Address:F4-5, #17 Building, Chuang Yi Yuan, No.6 Guanghua East Street, Nanjing, 210007 P.R.China

Relevant to this article

Highly enantioselective enzymatic resolution of aromatic β-amino acid amides with Pd-catalyzed racemization

Doi:10.1016/j.tetasy.2013.09.022
(2013)
Reactivity of amido ligands on a dinuclear Ru(II) center: Formation of imido complexes and C-N coupling reaction with alkyne

Doi:10.1021/ja047920s
(2004)
New approaches towards the synthesis of the side-chain of mycolactones A and B

Doi:10.1039/b505980a
(2005)
A SIMPLE SYNTHESIS OF THIOL ESTERS FROM COPPER-I-MERCAPTIDES AND ACYL CHLORIDES

Doi:10.1016/S0040-4039(00)92877-6
(1980)
The discovery of potent, orally bioavailable pyrimidine-5-carbonitrile-6- alkyl CXCR2 receptor antagonists

Doi:10.1016/j.bmcl.2014.06.011
(2014)
Design and synthesis of a novel series of cyanoindole derivatives as potent γ-secretase modulators

Doi:10.1016/j.bmcl.2019.05.023
(2019)

Article Doi