Scholarly article on ortho-t-butyloxyphenyllithium 66183-92-4 from Journal of Organometallic Chemistry p. 217

DOI: 10.1016/0022-328X(68)80044-0

Source and publish data:

Journal of Organometallic Chemistry p. 217 (1968)

Update date:2022-08-05

Topics:

Authors:

Shirley Shirley

Hendrix Hendrix

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

Article abstract of DOI:10.1016/0022-328X(68)80044-0

Full text of DOI:10.1016/0022-328X(68)80044-0

Products guided by the article

Product name:ortho-t-butyloxyphenyllithium

Cas No:66183-92-4

R&D Labs maybe for 66183-92-4

ZK Biochem Group Co., Ltd

Contact:+86-532-80762375

Address:No. 6, Hongkong Middle Road, Qingdao, China
Zipont chem(wuhan）Tech co.，Ltd

Contact:+86-27-87587198

Address:wuhan
Chongqing Changfeng Chemical Co., Ltd.

website:http://www.changfengchem.com

Contact:+86-23-67896333

Address:30th Floor, Longhu Ziduxingzuo Building A, 1st Branch,YuSong Rd., Yubei District, Chongqing, China
HEBEI BRANT PHARMACEUTICAL

Contact:+86-0311-84455288-844

Address:Mayu Industrial Park, Jinzhou, Hebei, China.
Taiwan Surfactant Corp.

Contact:886 2 2541 0022

Address:8 Fl., No. 11, Sec. 1, Chung Shan North Rd., Taipei, Taiwan R.O.C.

Relevant to this article

Doi:10.1021/jo00413a028
(1978)
Synthesis of tetrasubstituted ozonides by the Griesbaum coozonolysis reaction: Diastereoselectivity and functional group transformations by post-ozonolysis reactions

Doi:10.1021/jo040171c
(2004)
Synthesis, Biological Evaluation and Docking Study of New Pyrimidine Compounds as Anticancer Agents

Doi:10.1055/a-1306-0202
(2021)
Highly potent PDE4 inhibitors with therapeutic potential

Doi:10.1016/j.bmcl.2003.09.087
(2004)
Acyclic, achiral enamide nucleoside analogues. The importance of the C=C bond in the analogue for its ability to mimic natural nucleosides

Doi:10.1039/b307394g
(2003)
Doi:10.1039/c39750000819
(1975)

Article Doi

DOI: 10.1016/0022-328X(68)80044-0