Amino acids and peptides. 13. Preparation of active pyridyl-(3)-ester N-protected amino acids and peptides as well as their use in peptide synthesis

DOI: 10.1002/jlac.19656900117

Source and publish data:

Justus Liebigs Annalen der Chemie p. 177 - 181 (1965)

Update date:2022-07-29

Topics:

Authors:

Taschner

Rzeszotarska

Lubiewska

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

Article abstract of DOI:10.1002/jlac.19656900117

Full text of DOI:10.1002/jlac.19656900117

Products guided by the article

Product name:Formyl-Phe-pyridyl-⁽³⁾-ester

Cas No:5276-56-2

R&D Labs maybe for 5276-56-2

Jining Shengrun Chemical Industry Co., Ltd.

Contact:+86-537-7121666 ,

Address:West Ring Road,Wenshang County Shandong Province
Shandong Xiangde Biotechnology Co., Ltd

Contact:+86 -15066639877

Address:Sanba street
Liaoyang Xinyou Chemical Products Co.,Ltd.

Contact:+86-419-5165433 13604191870

Address:Huishang Road6-1, Hongwei District, Liaoyang, Liaoning, China
Suzhou ATL Chemical Co.,ltd

Contact:+86-0512-69209969

Address:Room 317,Lushan Road,Suzhou New District,Jiangsu Province,China.
H&Y International Group Ltd

Contact:+86-571-86491666

Address:SHI XIANG ROAD

Relevant to this article

Synthesis of Monofluoromethyl Selenoethers of Aryl and Alkyl from Organoselenocyanate via One-Pot Reaction

Doi:10.1002/adsc.201900480
(2019)
A direct alkylation route to branched derivatives of suberoylanilide hydroxamic acid (SAHA), a potent non-selective inhibitor of histone deacetylases

Doi:10.1016/j.tet.2016.11.039
(2016)
Enantioselective construction of quaternary stereogenic carbon atoms by the lewis base catalyzed additions of silyl ketene imines to aldehydes

Doi:10.1002/chem.201403342
(2014)
Doi:10.1016/0040-4020(73)80246-7
(1973)
Doi:10.1021/jo00889a016
(1975)
Doi:10.1002/ardp.19743070605
(1974)

Article Doi