Scholarly article on 6,6-dimethyl-5-oxo-2-phenyl-3-p-tolyl-heptanoic acid methyl ester 1071576-47-0 from Journal of the American Chemical Society p. 4350,4352

DOI: 10.1021/ja01363a012

Source and publish data:

Journal of the American Chemical Society p. 4350,4352 (1931)

Update date:2022-07-30

Topics:

Authors:

Avery Avery

Hall Hall

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

Article abstract of DOI:10.1021/ja01363a012

Full text of DOI:10.1021/ja01363a012

Products guided by the article

Product name:6,6-dimethyl-5-oxo-2-phenyl-3-p-tolyl-heptanoic acid methyl ester

Cas No:1071576-47-0

R&D Labs maybe for 1071576-47-0

Chen jie

Contact:027-87677569

Address:Room 2203, yujingmingmen Buidling One, xiongchu Road, wuhan city, hubei province, China
Chengdu Sino-Strong Pharmaceutical Co.,Ltd.

website:http://www.sino-strong.com.cn

Contact:+86-28-82666753

Address:459 West haike road,Cross-straits technological industry park, Wenjiang district,Chengdu, P.R.China
Wuhan Hanye Chemical New Material Co.,Ltd

Contact:+86-27-85308141

Address:LiuDian, Panlongcheng Economic Development Zone, HuangPi district, Wuhan, Hubei 430311 P.R.China
KA-SHING Business Trade Macau Co., Ltd.

Contact:00853-28430045

Address:23rd Floor, Block 3 La Cite, Areia Preta, Macao
Beijing Mashi Fine Chemical Co.,Ltd.

Contact:+86-10-61271592

Address:Room 506, Section B, Kaichi Mansion, Industrial Development

Relevant to this article

Identification of a nonbasic, nitrile-containing cathepsin K inhibitor (MK-1256) that is efficacious in a monkey model of osteoporosis

Doi:10.1021/jm800610j
(2008)
Kinetic Resolution of β-Hydroxy Carbonyl Compounds via Enantioselective Dehydration Using a Cation-Binding Catalyst: Facile Access to Enantiopure Chiral Aldols

Doi:10.1021/acs.orglett.8b00547
(2018)
(Benzenethiolato-S)(4-tert-butylpyridine-N)bis(dimethylglyoximato-N,N') cobalt(III) and (4-tert-butylpyridine-N)bis(dimethylglyoximato-N,N')(4-methoxybenzenethiolato-S) cobalt(III)

Doi:10.1107/S0108270198001693
(1998)
A Versatile Method to Prepare Difluorinated Primary Alcohols and Its Application to the Syntheses of Novel Acyclic Fluorinated Nucleosides

Doi:10.1016/j.tetlet.2013.10.037
(2013)
Orthoamide, LXI [1]. A new, efficient procedure for the synthesis of orthoamide derivatives of alkyne carboxylic acids

Doi:10.1515/znb-2005-0217
(2005)
Convenient reduction of azobenzenes and azoxybenzenes to hydrazobenzenes by sodium dithionite using dioctylviologen as an electron transfer catalyst

Doi:10.1016/S0040-4039(96)01451-7
(1996)

Article Doi

DOI: 10.1021/ja01363a012

Source and publish data: