A new synthesis of pyrocin and related compounds

DOI: 10.1246/bcsj.50.1133

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1133 - 1136 (1977)

Update date:2022-09-26

Topics:

Authors:

Takeda Takeda

Sakai Sakai

Shinohara

Tsuboi Tsuboi

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

Article abstract of DOI:10.1246/bcsj.50.1133

Full text of DOI:10.1246/bcsj.50.1133

Products guided by the article

Product name:3-Furancarboxylic acid, 4,5-dihydro-5,5-dimethyl-4-(2-methyl-1-propenyl)-2-phenyl-, ethyl ester

Cas No:63832-27-9

R&D Labs maybe for 63832-27-9

Synchem Pharma Co.,Ltd(expird)

Contact:+0086-21-61984905-1

Address:Building 60,Zimian Park, LongYang industrial Area, 1515Nong，Yuandong Road Fengxian District, Shanghai ,China
Sinochem Jiangsu Co.,Ltd.

Contact:86-25-51817806

Address:No. 216, middle longpan road, jincheng tower, floor 21-22, nanjing ,china
QINGDAO TAOSIGN INTERNATIONAL TRADE CO.,LIMITED

Contact:+86-0532-82683616

Address:RM1402, Doublestar Seacoase 7#, No. 5 Guizhou Road, Qingdao, Shandong, China
HANGZHOU YUNUO CHEMICAL CO.,LTD

website:http://www.yunuochem.com

Contact:0571-83715115

Address:hangzhou
PharmaResources(Kaiyuan)CO,.Ltd

Contact:+86-21-50720028

Address:No.3, Beihuan Road, Economic Development District, Kaiyuan City, Tieling City, Liaoning Province, China 112300

Relevant to this article

Doi:10.1021/ja01632a101
(1954)
Doi:10.1016/0040-4020(77)80039-2
(1977)
Synthesis and crystal structure of Ru3(μ3-NPh)(μ-DPPM)(CO)8

Doi:10.1016/0022-328X(88)80678-8
(1988)
β-Adrenergic blocking agents. 17. 1-Phenoxy-3-phenoxyalkylamino-2-propanols and 1-alkoxyalkylamino-3-phenoxy-2-propanols

Doi:10.1021/jm00222a022
(1977)
A lipid-lipase aggregate with ether linkage as a new type of immobilized enzyme for enantio-selective hydrolysis in organic solvents

Doi:10.1248/cpb.40.318
(1992)
Synthesis, structural and vibrational investigation on 2-phenyl-N-(pyrazin- 2-yl)acetamide combining XRD diffraction, FT-IR and NMR spectroscopies with DFT calculations

Doi:10.1016/j.saa.2014.07.004
(2015)

Article Doi