Studies on peptides. CXXIII. Preparations of nine peptide fragments for the synthesis of human corticotropin releasing factor (hCRF)

DOI: 10.1248/cpb.32.4786

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 4786 - 4796 (1984)

Update date:2022-08-04

Topics:

Authors:

Fujii Fujii

Nomizu Nomizu

Akaji Akaji

Shimokura

Katakura

Yajima Yajima

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

Article abstract of DOI:10.1248/cpb.32.4786

Full text of DOI:10.1248/cpb.32.4786

NII-Electronic Library Service

Products guided by the article

Product name:H-Arg(Mts)-Lys(Z)-Leu-OMe

Cas No:90709-71-0

R&D Labs maybe for 90709-71-0

Jintan City Mego Chemical Co., Ltd

Contact:+86-0519-82814387

Address:23# Dengguan Town, Jintan, Jiangsu Province, China
Weifang Ocean Trading Co., Ltd.

Contact:+86-536-2081155

Address:Room2606, Yuqing Building, 518#, Yuquan Road, High-tech Development Zone, Weifang City, Shandong Province, China
Frapp's Chemical (NFTZ) Co.,Ltd

Contact:+86-576-86137892

Address:General Chamber of Commercial Building, 159 Wanchang Middle Road, Wenling, Zhejiang, China
Wuhan Fortuna Chemical Co.,Ltd

website:http://www.fortunachem.com

Contact:86-27-59207850

Address:Add: Room 2015, No.2 Building, Kaixin Mansion No.107 Jinqiao Avenue, Wuhan, China
Lanzhou SchiffChem Co.,Ltd

Contact:86-931-8272767

Address:Room 602, No.461, Nanchang Road, Chengguan District, Lanzhou City, China PRC

Relevant to this article

3-Chloro-2-(phenylsulfinyl)-1-propene and 3-Chloro-2-(phenylsulfonyl)-1-propene: Preparation and Utility as Reagents for α,α'-Annelation of Cyclic Ketones

Doi:10.1021/jo00191a017
(1984)
Germanium and Silicon Linking Strategies for Traceless Solid-Phase Synthesis

Doi:10.1021/jo961889y
(1997)
An efficient method for the reductive conversion of acyclic esters to ethers via a TMS-protected acetal

Doi:10.1016/j.tetlet.2017.06.043
(2017)
Studies on the hydrogenolysis of benzyl ethers

Doi:10.1016/j.tetlet.2006.05.109
(2006)
Doi:10.1139/v64-010
(1964)
Stereoselective synthesis of the C1-C10 fragment of rhizoxin D

Doi:10.1016/j.tetlet.2006.06.046
(2006)

Article Doi