IMPROVED METHODS OF SYNTHESIS OF VALINOMYCINS

DOI: 10.1016/S0040-4039(00)99557-1

Source and publish data:

Tetrahedron Letters p. 1695 - 1698 (1989)

Update date:2022-08-03

Topics:

Authors:

Dory, Yves L.

Mellor, John M.

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

Article abstract of DOI:10.1016/S0040-4039(00)99557-1

Linear depsipeptides have been efficiently cyclised to give cyclodepsipeptide valinomycin analogues via a protocol using activated pentafluorophenyl esters in conjunction with deprotection of a benzylcarbamate by in situ hydrogenolysis.Valinomycins having

Full text of DOI:10.1016/S0040-4039(00)99557-1

Products guided by the article

Product name:Cyclo-(L-Val-L-Hyiv-L-Val-L-Hyiv)3

Cas No:125827-11-4

R&D Labs maybe for 125827-11-4

Tai zhou world Pharm & Chem Co., Ltd

Contact:+86-576-85301198

Address:Rome 1001,wangjiang plaza,unti 2,jinshan east Road linhai,zhejiang,china
Cangzhou Senary Chemical Science-tech Co., Ltd

Contact:+86-317-3563899, 3563699

Address:168 Jinde Road, Cangzhou, Hebei, China
Shandong Ailitong New Material Co.,Ltd

Contact:+86-536-3226266

Address:zhongjia village, putong town , qingzhou city,Shandong Province,China
Hefei Highzone Fine Chemical S&T CO.,LTD

Contact:86-0551-63663560

Address:room 1801 NO. 24 Shuguang RD.
Lianyungang Ningkang Chemical Co., Ltd

Contact:.+86-518-88588008

Address:http://www.chemnk.com

Relevant to this article

Synthesis, characterization, spectral and catalytic activity of tetradentate (NNNO) azo-imine Schiff base copper(II) complexes

Doi:10.1016/j.ica.2018.04.042
(2018)
Doi:10.1039/jr9580004064
(1958)
Studies on the syntheses of heterocyclic compounds. Part DXCVII (1). A synthesis of dienone analogs by electrolytic oxidation

Doi:10.1002/jhet.5570120218
(1975)
Non-defluorinative electrochemical silylation of ethyl trifluoroacetate: A practical synthesis of trifluoroacetyltrimethylsilane via its ethyltrimethylsilyl ketal

Doi:10.1016/S0040-4039(03)00745-7
(2003)
One-pot synthesis of N-substituted pantolactams from pantolactone

Doi:10.1016/S0040-4020(03)00156-X
(2003)
Doi:10.1002/hlca.19750580423
(1975)

Article Doi