Enantiospecific Preparation of the Lactone Fragment of Murisolin

DOI: 10.1016/S0957-4166(00)82115-1

Source and publish data:

Tetrahedron Asymmetry p. 347 - 350 (1991)

Update date:2022-09-26

Topics:

Authors:

Harmange, Jean-Christophe

Figadere, Bruno

Hocquemiller, Reynald

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

Article abstract of DOI:10.1016/S0957-4166(00)82115-1

Both enantiomers (R) and (S) of the functionalized unsaturated γ-lactone moiety of the acetogenin murisolin have been enantiospecifically synthezised from L and D-glutamic acid respectively.

Full text of DOI:10.1016/S0957-4166(00)82115-1

Products guided by the article

Product name:2(3H)-Furanone, dihydro-5-methyl-3-(2-propenyl)-, cis-

Cas No:93757-77-8

R&D Labs maybe for 93757-77-8

NOVASYNCS CO., LTD

Contact:0512-63006287

Address:no.88.YISHENG Road,etdz-WUJIANG,SUZHOU,CHINA
HEZE KINGVOLT CHEMICAL CO., LTD

Contact:86-573-82118911

Address:Juancheng Industry Park
Springchem New Material Technology Co.,Limited

website:http://www.spring-chem.com

Contact:86-21-62885108

Address:602B, Building 1, No. 641, Tianshan Road
shijiazhuang alkay chemicals co..ltd(expird)

Contact:86-311-67692035

Address:2601,juntang building,qiaodong district,shijiazhuang
Hangzhou Sartort Biopharma Co., Ltd

website:http://www.sartort.com

Contact:86-571-87039693

Address:No. 57, Tech Park Road, Hangzhou, Zhejiang, China

Relevant to this article

The first silver catechol complexes: Crystal structures of triphenylphosphine stabilized silver tetra-bromo and tetra-chloro-catechols

Doi:10.1016/j.poly.2006.01.009
(2006)
p-Fluorobenzoyl Chloride for Characterization of Active Hydrogen Functional Groups by Fluorine-19 Nuclear Magnetic Resonance Spectrometry

Doi:10.1021/ac00276a014
(1984)
Optically active: Microwave-assisted synthesis and characterization of l-lysine-derived poly (amide-imide)s

Doi:10.1007/s00726-010-0767-0
(2011)
Doi:10.1021/jo01052a047
(1962)
New expanded-ring NHC platinum(0) complexes: Synthesis, structure and highly efficient diboration of terminal alkenes

Doi:10.1016/j.jorganchem.2020.121140
(2020)
Doi:10.1016/S0040-4020(01)91187-1
(1984)

Article Doi