Scholarly article on 2-Aethyl-2-methyl-1-butylbrosylat 14248-16-9 from Journal of the American Chemical Society p. 5816 - 5820

DOI: 10.1021/ja00976a023

Source and publish data:

Journal of the American Chemical Society p. 5816 - 5820 (1966)

Update date:2022-08-02

Topics:

Authors:

Heidke,R.L.

Saunders,W.H.

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

Article abstract of DOI:10.1021/ja00976a023

Full text of DOI:10.1021/ja00976a023

Products guided by the article

Product name:2-Aethyl-2-methyl-1-butylbrosylat

Cas No:14248-16-9

R&D Labs maybe for 14248-16-9

Shijiazhuang Sdyano Fine Chemical Co., Ltd

Contact:+86-311-89830448

Address:NO.48 Ta Nan Road,Yuhua District,Shijiazhuang,Hebei,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
AstaTech ( Chengdu) BioPharmaceutical Corp.

website:http://www.astabiochem.cn/

Contact:+86-15198215156-15198215156

Address:SICHUAN CHENGDU
BIOS CHEMICALS

Contact:+33-5-34012600

Address:28 ZA des Pignès
CHEM PLUS

Contact:0027-717-456976

Address:2ND FLOOR, 325 VAUSE ROAD, OVERPORT, 4001, SOUTH AFRICA

Relevant to this article

Bistability of Fc-PTM-Based dyads: The role of the donor strength

Doi:10.1021/cm400147p
(2013)
Potent BRAF kinase inhibitors based on 2,4,5-trisubstituted imidazole with naphthyl and benzothiophene 4-substituents

Doi:10.1016/j.bmc.2012.12.035
(2013)
Enantioselective Arylation of Benzylic C?H Bonds by Copper-Catalyzed Radical Relay

Doi:10.1002/anie.201902191
(2019)
Application of a stereoselective rhodium(II)-catalyzed oxonium ylide formation-[2,3]-sigmatropic rearrangement of an α-diazo-β-keto ester to the synthesis of 2-epi-cinatrin C₁ dimethyl ester

Doi:10.1055/s-0032-1317694
(2013)
Double palladium-catalyzed synthesis of azepines

Doi:10.1055/s-0032-1317667
(2013)
Efficient and practical synthesis of enantioenriched 2,3-dihydropyrroles through gold-catalyzed anti-Markovnikov hydroamination of chiral homopropargyl sulfonamides

Doi:10.1039/c4cc09245g
(2015)

Article Doi

DOI: 10.1021/ja00976a023