Scholarly article on 2-(α-hydroxy-4-iodo-benzyl)-cyclohexanone 100714-25-8 from Journal of the American Chemical Society p. 1147,1151

DOI: 10.1021/ja01587a016

Source and publish data:

Journal of the American Chemical Society p. 1147,1151 (1956)

Update date:2022-08-03

Topics:

Authors:

Huitric Huitric

Kumler Kumler

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

Article abstract of DOI:10.1021/ja01587a016

Full text of DOI:10.1021/ja01587a016

Products guided by the article

Product name:2-(α-hydroxy-4-iodo-benzyl)-cyclohexanone

Cas No:100714-25-8

R&D Labs maybe for 100714-25-8

Tocopharm Co., Ltd.

Contact:+86-021-6989-5597

Address:No.80 Yichuan Rd., Putuo District,Shanghai,P.R.China
Zhenjiang Haitong Chemical Industry Co., Ltd.

Contact:+86 (511) 8448-0369

Address:Baoyan Town, Dantu District, Zhenjiang City, Jiangsu, China
Beijing ZhongDaXinHe Chemical Product Co.,Ltd(expird)

Contact:010-52876516

Address:tongzhoubeiyuan
KODI CHEMICAL CO., LTD

Contact:021

Address:Pudong
HUNAN OUYA BIOLOGICAL CO.,LTD

Contact:+8613400661290

Address:No 908,Kangwan Rd, Liuyang Economic

Relevant to this article

Biotransformation of daclatasvir in vitro and in nonclinical species: Formation of the main metabolite by pyrrolidine d-Oxidation and Rearrangements

Doi:10.1124/dmd.115.068866
(2016)
Tandem asymmetric allylboration-alkene metathesis: A novel strategy for the synthesis of trans-disubstituted homoallylic alcohols

Doi:10.1039/CC9960002229
(1996)
Synthesis and biological evaluation of carbon-substituted C-4 derivatives of podophyllotoxin

Doi:10.1139/v96-187
(1996)
Efficient synthesis of D-[5-¹³C]ribose from D-ribose and its conversion into [5'-¹³C]nucleosides

Doi:10.1016/0040-4039(96)01770-4
(1996)
Syntheses, pharmacological evaluation and molecular modelling of substituted 6-alkoxyimidazo<1,2-b>pyridazines as new ligands for the benzodiazepine receptor

Doi:10.1016/0223-5234(96)85873-9
(1996)
Luminescent Ce(III) Complexes as Stoichiometric and Catalytic Photoreductants for Halogen Atom Abstraction Reactions

Doi:10.1021/jacs.5b05411
(2015)

Article Doi

DOI: 10.1021/ja01587a016