Synthesis of cyclic depsipeptides and peptides via direct amide cyclization

DOI: 10.1002/hlca.19970800312

Source and publish data:

Helvetica Chimica Acta p. 748 - 766 (1997)

Update date:2022-09-26

Topics:

Authors:

Villalgordo, Jose M.

Heimgartner, Heinz

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

Article abstract of DOI:10.1002/hlca.19970800312

The 2,2-disubstituted 2H-azirin-3-amines 7 (2,2-disubstituted 3-amino-2H-azirines) were used as amino-acid synthons in the preparation of medium-sized cyclic depsipeptides and peptides derived from salicylic acids 6 and anthranilic acid 19, respectively.

Full text of DOI:10.1002/hlca.19970800312

Products guided by the article

Product name:Benzamide, N-[1,1-dimethyl-2-(methylphenylamino)-2-oxoethyl]-2-hydroxy-

Cas No:192046-36-9

R&D Labs maybe for 192046-36-9

Tianjin Pharmacn Medical Technology Co.,Ltd.

Contact:86-22-60122566ext.866(English),23359620

Address:Green Industrial Base, 6 Haitaifazhan Sixth Rd., Huayuan Industrial Area, Tianjin, 300384, China
SHANGHAI BIOSUNDRUG CO.,LTD.

Contact:86-21-34622192，13917187091，21-34622765

Address:No. 500 Caobao Road Shanghai P.R China
Qingdao XinYongAn Chemicals Co., Ltd

Contact:+86-532-81107967

Address:Chengyang dual-port industrial park by the sea，Qingdao
Shanghai Gsyn Chemical Co.,Ltd.

Contact:86-021-67158290

Address:86-021-67158291
Henan Harvest Chem Co., Ltd

Contact:+86-371-86058576

Address:NO.32, Jingsan Road, Zhengzhou, China

Relevant to this article

2-carbomethoxy-3-aryl-8-oxabicyclo[3.2.1]octanes: Potent non-nitrogen inhibitors of monoamine transporters

Doi:10.1021/jm9703045
(1997)
Resolution of racemic carboxylic acid derivatives by Ti-TADDOLate mediated esterification reactions a general method for the preparation of enantiopure compounds

Doi:10.1016/S0040-4020(97)00456-0
(1997)
Conformational dependence of substituent effects in the solvolyses of the 1,1-diphenyl-2,2,2-trifluoroethyl system

Doi:10.1002/poc.489
(2002)
Synthesis of pyrrolyl-, indolyl-, and carbazolylphosphanes and their catalytic application as ligands in the hydroformylation of 2-pentene

Doi:10.1002/1099-0690(200110)2001:20<3871::AID-EJOC3871>3.0.CO;2-V
(2001)
The discovery of highly potent thp derivatives as octn2 inhibitors: From structure‐based virtual screening to in vivo biological activity

Doi:10.3390/ijms21197431
(2020)
An anion-induced regio- and chemoselective acylation and its application to the synthesis of an anticancer agent

Doi:10.1021/ol016809d
(2001)

Article Doi