Scholarly article on 8-iodocoumarin 18438-99-8 from Journal of the American Chemical Society p. 1242,1244

DOI: 10.1021/ja01060a057

Source and publish data:

Journal of the American Chemical Society p. 1242,1244 (1964)

Update date:2022-08-02

Topics:

Authors:

Holmes Holmes

Robins Robins

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

Article abstract of DOI:10.1021/ja01060a057

Full text of DOI:10.1021/ja01060a057

Products guided by the article

Product name:8-iodocoumarin

Cas No:18438-99-8

R&D Labs maybe for 18438-99-8

Jitat Company Ltd

Contact:852-27701081

Address:Room 2509, New Tech Plaza, 34 Tai Yau St., San Po Kong, HK
Hangzhou Zyter Biological & Chemical Technology Co., Ltd.

website:http://www.zyterpharm.com

Contact:+86-18858184290

Address:West Wenyi Road, Cangqian, Yuhang
Nantong Kaixin Pharma Chemical Co.,Ltd.

Contact:86-513-85250786

Address:2-1103 Huachen Mansion, 111 Gongnong Road,Nantong, Jiangsu, China
Hawks Chemical

Contact:+44 (0)161 367 9441

Address:
UNION PHARMPRO CO.,LTD

Contact:18710867521(wechat)

Address:Rm10516,Galaxy Tech Building #2,No.25 Tangyan Rd,Hi-Tech Zone,Xi'an, China

Relevant to this article

Doi:10.1016/S0040-4039(01)96550-5
(1971)
Liquid hydrogenation of maleic anhydride with Pd/C catalyst at low pressure and temperature in batch reactor

Doi:10.1166/jnn.2015.8349
(2015)
Rhodium-catalyzed asymmetric arylation of imines with organostannanes. Asymmetric synthesis of diarylmethylamines [14]

Doi:10.1021/ja9927220
(2000)
Palladium-Catalyzed Cyclobutanation of Aryl Sulfonates through both C-O and C-H Cleavage

Doi:10.1021/acs.organomet.0c00338
(2020)
Fluorine containing heterocyclic compounds: Synthesis of 6-substituted-2-substituted-aryl-1,2,4-triazolo[5,1-b] 1,3,5-thiadiazin-7-one derivatives

Doi:10.1016/S0022-1139(00)00287-6
(2000)
One-pot synthesis of 2-methyl-1,5-diaromatic-1H-pyrroles from styrene, acetone and arylamines using TBHP, copper(II) trifluoromethanesulfonate and sulfamic acid

Doi:10.1016/j.tetlet.2017.12.031
(2018)

Article Doi

DOI: 10.1021/ja01060a057