STRUKTUR UND SYNTHESE VON N-(ACETOXY)-JASMONOYLPHENYLALANINMETHYLESTER AUS PRAXELIS CLEMATIDEA

DOI: 10.1016/S0040-4020(01)83506-7

Source and publish data:

Tetrahedron p. 2537 - 2540 (1984)

Update date:2022-08-04

Topics: Experimental terms SYNTHESE STRUKTUR

Authors:

Bohlmann, Ferdinand

Wegner, Peter

Jakupovic, Jasmin

King, Robert M.

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

Article abstract of DOI:10.1016/S0040-4020(01)83506-7

From Praxelis clematidea a phenylalanine derivative has been isolated, its structure being elucidated by spectroscopic methods and confirmed by synthesis.

Full text of DOI:10.1016/S0040-4020(01)83506-7

Products guided by the article

Product name:(-)N-(12-Acetoxy-9,10-dehydrojasmonoyl)-phenylalaninmethylester

Cas No:91991-54-7

R&D Labs maybe for 91991-54-7

HAINAN JINYING IMPORT AND EXPORT CO. LTD

Contact:+86-898-32875423

Address:A SECTION 19TH FL, TIMES SQUARE, NO.2 GUO MAO AVENUE HAIKOU, HAINAN, P. R. OF CHINA
Shijiazhuang Haitian Amino Acid Co., Ltd.

Contact:+86-311-88908111

Address:Shijiazhuang Hebei province,China
Taizhou volsen chemical Co., Ltd

website:http://www.volsenchem.com

Contact:+86-576-88869393

Address:Jiaojiang District, Taizhou, Zhejiang, China.
VanderArk International Limited

Contact:86-10-82437576

Address:Qing He
Suzhou Wedo Chemicals Co., Ltd.

Contact:86 512 58100425

Address:Zonger Road, DongSha Industry Park , Zhangjiagang, Jiangsu, China

Relevant to this article

CYANO ANALOGS OF PHENOLIC NITROGEN MUSTARDS.

Doi:10.1021/jm00335a027
(1964)
Doi:10.1016/0040-4020(68)88054-8
(1968)
Ni(OAc)₂: A highly efficient catalyst for the synthesis of enaminone and enamino ester derivatives under solvent-free conditions

Doi:10.1002/aoc.1667
(2010)
Preparation and allylation of enamides and enecarbamates generated via iron(0) reduction of oximes and derivatives

Doi:10.1055/s-2006-942513
(2006)
Lipid tucaresol as an adjuvant for methamphetamine vaccine development

Doi:10.1039/c4cc00682h
(2014)
Dioxygenase-catalysed dihydroxylation of arene cis-dihydrodiols and acetonide derivatives: A new approach to the synthesis of enantiopure tetraoxygenated bioproducts from arenes

Doi:10.1039/b612191h
(2006)

Article Doi