Scholarly article on Bis--disulfid 21293-56-1 from Journal of the American Chemical Society p. 5548 - 5552

DOI: 10.1021/ja01022a041

Source and publish data:

Journal of the American Chemical Society p. 5548 - 5552 (1968)

Update date:2022-08-05

Topics:

Authors:

Corey,E.J.

Durst,T.

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

Article abstract of DOI:10.1021/ja01022a041

Full text of DOI:10.1021/ja01022a041

Products guided by the article

Product name:Bis--disulfid

Cas No:21293-56-1

R&D Labs maybe for 21293-56-1

Goldwills Pharmaceuticals Co., Ltd.

Contact:0916-2237889 13991621155

Address:North Suburb of Hanzhong city, Shaanxi Province
Sdow

website:http://www.sdowchem.com

Contact:86-135-2193 7483

Address:8-106 taiyue building
Nanjing Capatue Chemical Co., Ltd

Contact:+86-25-86371192 +86-025-85720158

Address:No.20 Jiangjun Avenue, Jiangning Economic & Technical Development Zone
puyang hongda shengdao new material co.,ltd.

Contact:+86-393- 4896278

Address:No.29 East Zhongyuan Road
sichuan tiancai fine co LTD.

website:http://www.tcfinechem.com/

Contact:18681346930

Address:baifu town,whou district

Relevant to this article

Kinetic and thermodynamic aspects in the 1,3-dipolar cycloaddition of five-membered cyclic nitrones to α,β-unsaturated γ- and δ-lactones

Doi:10.1016/j.tetasy.2007.04.015
(2007)
Synthesis of enantiopure cyclopentitols and aminocyclopentitols mediated by oxyselenenylation of cyclopentene with (R,R)-hydrobenzoin

Doi:10.1016/S0040-4039(98)01377-X
(1998)
A route to Z-enediynes via Pd catalyzed alkyne additions

Doi:10.1016/S0040-4039(98)01392-6
(1998)
Chemo-Enzymatic Metathesis/Aromatization Cascades for the Synthesis of Furans: Disclosing the Aromatizing Activity of Laccase/TEMPO in Oxygen-Containing Heterocycles

Doi:10.1021/acscatal.9b02452
(2019)
Synthesis of fully and partially benzylated glycosyl azides via thioalkyl glycosides as precursors for the preparation of N-glycopeptides

Doi:10.1016/S0040-4039(98)01540-8
(1998)
Analysis and Identification of 2′-Deoxyadenosine-Derived Adducts in Lung and Liver DNA of F-344 Rats Treated with the Tobacco-Specific Carcinogen 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone and Enantiomers of its Metabolite 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol

Doi:10.1021/acs.chemrestox.8b00056
(2018)

Article Doi

DOI: 10.1021/ja01022a041