A SYNTHESIS OF OXYTOCIN.

DOI: 10.1246/bcsj.38.120

Source and publish data:

Bulletin of the Chemical Society of Japan p. 120 - 123 (1965)

Update date:2022-08-04

Topics:

Authors:

SAKAKIBARA

NOBUHARA

SHIMONISHI

KIYOI KIYOI

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

Article abstract of DOI:10.1246/bcsj.38.120

Full text of DOI:10.1246/bcsj.38.120

Products guided by the article

Product name:L-Cysteine, S-[(4-methoxyphenyl)methyl]-N-[(phenylmethoxy)carbonyl]-

Cas No:3081-32-1

R&D Labs maybe for 3081-32-1

Qingdao S. H. Huanyu Imp. & Exp. Co., Ltd.

Contact:86-532-88250866

Address:Room 615, World Trade Centre Building B, Hongkong Middle Roda 6#, Qingdao, Shandong, China
Beijing Apis Biotechnology Co., Ltd.

Contact:86-010-67856775-8551

Address:NO.4PUHUANGYU ROAD,FENTAI DISTRICT, BEIJING, CHINA
Dongguan Albiya Energy Science and Technology Co.,Ltd

Contact:+86-769-22181286

Address:Huanan Industial Park, Dongguan,China
Shanghai Mio Chemical Co., Ltd

Contact:0086 21- 64401188-622

Address:16 Floor NO.2 Jiefang Building, No. 4855 Dushi Road, 201100 Shanghai, P.R.China
Hubei Xiangxi Chemical Industry Co.,Ltd

Contact:+86-710-3454830

Address:No.7, Daqing East Road, Xiangfan City, Hubei Province, China

Relevant to this article

Doi:10.1021/ja01591a065
(1956)
Synthesis of (1S,3aS)-8-(2,3,3a,4,5,6-hexahydro-1H-phenalen-1-yl)-1-phenyl-1,3,8-triaza-sp iro[4.5]decan-4-one, a potent and selective orphanin FQ (OFQ) receptor agonist with anxiolytic-like properties

Doi:10.1016/S0223-5234(00)00171-9
(2000)
Solution-phase synthesis of the fluorogenic TGase 2 acyl donor Z-Glu(HMC)-Gly-OH and its use for inhibitor and amine substrate characterisation

Doi:10.1016/j.ab.2020.113612
(2020)
Enantioselective synthesis of alkyl-branched alkanes. Synthesis of the stereoisomers of 7,11-dimethylheptadecane and 7-methylheptadecane, components of the pheromone of Lambdina species

Doi:10.1021/jo0055436
(2000)
Absolute asymmetric phthalide synthesis via the solid-state photoreaction of N,N-disubstituted 2-benzoylbenzamides involving a radical pair intermediate [3]

Doi:10.1021/ja001064c
(2000)
Doi:10.1021/ja01130a056
(1952)

Article Doi