Scholarly article on 10-deuterio-5-(2,4,6-trimethyl-phenyl)-5,10-dihydro-dibenzo[b,e]borinine 33586-38-8 from Journal of Organometallic Chemistry p. 153 - 165

DOI: 10.1016/S0022-328X(00)81314-5

Source and publish data:

Journal of Organometallic Chemistry p. 153 - 165 (1974)

Update date:2022-08-05

Topics:

Authors:

van Veen,R.

Bickelhaupt,F.

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

Article abstract of DOI:10.1016/S0022-328X(00)81314-5

Full text of DOI:10.1016/S0022-328X(00)81314-5

Products guided by the article

Product name:10-deuterio-5-(2,4,6-trimethyl-phenyl)-5,10-dihydro-dibenzo[b,e]borinine

Cas No:33586-38-8

R&D Labs maybe for 33586-38-8

Shanghai Xinda Pharmaceuticals Co., Ltd.

Contact:86-21-33692333-8008

Address:999 Linxian Road, Jinshan Industrial Park, Shanghai, China
Alchemy industrial limited

Contact:+86-18200374913

Address:Hongmei Road, No. 99
Eastar Chemical Corporation

website:http://www.eastarchem.com/

Contact:1-800-898-2436

Address:1215 K Street, STE 1700
Shantou Baokang Pharmaceutical Co., Ltd.

Contact:+86-754-88873487

Address:5/F B Block Huangshan Bldg Huangshan Rd Shantou
Zibo Xiaoguang Chemical Material Co., Ltd

Contact:15954099116

Address:Boshan Development Zone

Relevant to this article

An Improved Synthesis of 2,7-Dihydroxytropone (3-Hydroxytropolone)

Doi:10.1055/s-1986-31713
(1986)
Doi:10.1021/ja00745a053
(1971)
The synthesis of β-peptides containing guanidino groups

Doi:10.1016/S0960-894X(01)00027-0
(2001)
New silylated iminophosphorano(amino)phosphines Me₃SiN=PPh₂N(r)PPh₂ (R = Et, ⁿPr, ⁿBu). Crystal and molecular structure of trimethylsilyliminophosphorano(propylamino)-diphenylphosphine Me₃SiN=PPh₂N(ⁿPr)PPh₂. Further oxidative derivatization with S, Se, and azides

Doi:10.1021/ic000878r
(2001)
Synthesis of 1,1′-methylenedi[(1R,1′R,3R,3′R,5R,5′R)-8-oxabicyc lo[3.2.1]oct-6-en-3-ol] and derivatives: Precursors of long-chain polyketides

Doi:10.1016/S0957-4166(00)00475-4
(2000)
Gold(I)-Catalyzed Glycosylation with Glycosyl Ynenoates as Donors

Doi:10.1021/acs.orglett.9b03851
(2019)

Article Doi

DOI: 10.1016/S0022-328X(00)81314-5