Scholarly article on 2,2,4,6,6-pentamethylcyclohexanone 29668-29-9 from Journal of the American Chemical Society p. 2273 - 2279

DOI: 10.1021/ja00762a017

Source and publish data:

Journal of the American Chemical Society p. 2273 - 2279 (1972)

Update date:2022-08-02

Topics:

Authors:

Walborsky,H.M.

Turner,L.M.

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

Article abstract of DOI:10.1021/ja00762a017

Full text of DOI:10.1021/ja00762a017

Products guided by the article

Product name:2,2,4,6,6-pentamethylcyclohexanone

Cas No:29668-29-9

R&D Labs maybe for 29668-29-9

Xi'an Terra Biochem Co. Ltd.

Contact:0086-29-88315623

Address:S711, Innovation Bldg No.25 Gaoxin 1st Rd, Xian P.R of China 710075
SuZhou Bichal Biological Technology CO.,LTD

Contact:+86-512-68051130

Address:NO.32 huoju road HI-TECH Industrial development zone SuZhou China
Ningbo Inno Pharmchem Co., Ltd.

Contact:86-574-87319282

Address:6F-5,NO.163 RUIQING RD.,NINGBO 315000 CHINA
Yurui(Shanghai)Chemical Co.,Ltd

Contact:0086 21-50456736

Address:No.3188 Xiupu Road,Shanghai
Shanghai Sungo Technology Chemical Co., Ltd

Contact:0086-21-51385579

Address:Room2010, F/20, Tonghua Plaza, NO 345 Jinxiang Road, Jinqiao Export Processing Zone, Shanghai, 201206 P.R.CHINA

Relevant to this article

An Efficient Approach to Regio- and Stereodefined Fully-Substituted Alkenylsilanes by Pd-Catalyzed Allenic C(sp³)?H Oxidation

Doi:10.1002/chem.201902962
(2019)
Synthesis of [³H₂]-(11S,17R)-11,17-dimethylhentriacontane: A useful tool for the study of the internalisation of communication pheromones of ant Camponotus vagus

Doi:10.1016/S0040-4020(00)00447-6
(2000)
Asymmetric synthesis of (-)-paroxetine using PLE hydrolysis

Doi:10.1016/S0040-4039(00)00942-4
(2000)
Total synthesis of (-)-CP-263,114 (phomoidride B) [8]

Doi:10.1021/ja001664b
(2000)
Synthesis of α-fluorocarboxylates from the corresponding acids using acetyl hypofluorite

Doi:10.1021/jo010677k
(2001)
Synthesis of actiketal, a glutarimide antibiotic

Doi:10.1016/S0040-4039(00)00928-X
(2000)

Article Doi

DOI: 10.1021/ja00762a017