Synthetic study on peptide antibiotic nisin. III. Synthesis of ring C

DOI: 10.1246/bcsj.63.1838

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1838 - 1840 (1990)

Update date:2022-09-26

Topics:

Authors:

Fukase Fukase

Kitazawa

Wakamiya

Shiba Shiba

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

Article abstract of DOI:10.1246/bcsj.63.1838

Full text of DOI:10.1246/bcsj.63.1838

Products guided by the article

Product name:Boc-3-Me-D-Cys(Trt)-Gly-OH*DCAH

Cas No:130226-65-2

R&D Labs maybe for 130226-65-2

Acros Pharmatech Limited

website:http://www.acrospharmatech.com

Contact:+1-3234804688

Address:Flat/RM 1502,Easey Commercial building 253-261 Hennessy Road,Wanchai，HongKong
Jinzhou Jiutai Pharmaceutical Co.,Ltd

Contact:+86-0416-5179890

Address:No.41, Taianli, Taihe District, Jinzhou, Liaoning
Shanghai Surseechem Co.,Ltd.

Contact:+86-21-61318535

Address:Building 29,No.2139 Xizha Road, Fengxian District, Shanghai
Hangzhou Showland Technology Co., Ltd.

Contact:86-571-88920516

Address:ROOM2118,NO.553,WENSAN ROAD,HANGZHOU,CHINA
A-Chem Technologies Co.,Ltd.

Contact:+86-512-69561895

Address:No.111, Building A4, 218 Xinghu Street, Suzhou Industrial Park, P. R. China

Relevant to this article

Asymmetric synthesis of α-alkyl α-selenocarbonyl compounds catalyzed by bifunctional organocatalysts

Doi:10.1021/ol200923p
(2011)
Self-organizing properties of monosubstituted sucrose fatty acid esters: The effects of chain length and unsaturation

Doi:10.1002/chem.200500773
(2006)
Syntheses of 2-(6'-Fluorobenzothiazol-2'-ylamino)-4, 6-(disubstituted thiouriedo)-1,3-pyrimidine derivatives as antimicrobial agents

Doi:10.1155/2011/820718
(2011)
Mild and efficient iodine-catalyzed direct substitution of hydroxy group of alcohols with c- and n-nucleophiles

Doi:10.2174/157017811794557787
(2011)
A new class of β-carboline alkaloid-peptide conjugates with therapeutic efficacy in acute limb ischemia/reperfusion injury

Doi:10.1016/j.ejmech.2011.01.021
(2011)
Structure-based design of potent human dihydroorotate dehydrogenase inhibitors as anticancer agents

Doi:10.1039/c6md00179c
(2016)

Article Doi