An efficient access to the enantiomers of α-methyl-4-carboxyphenylglycine via a hydantoin route using a practical variant of preferential crystallization. AS3PC (auto seeded programmed polythermic preferential crystallization)

DOI: 10.1016/S0957-4166(97)00349-2

Source and publish data:

Tetrahedron Asymmetry p. 2913 - 2920 (1997)

Update date:2022-08-05

Topics:

Authors:

Ndzie Ndzie

Cardinael

Schoofs Schoofs

Coquerel

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

Article abstract of DOI:10.1016/S0957-4166(97)00349-2

The enantiomers are obtained in preparative amounts without a resolving agent via the following sequence: hydantoin synthesis, resolution by entrainment, and ring cleavage by means of hydrolysis in basic conditions. The new variant of preferential crystal

Full text of DOI:10.1016/S0957-4166(97)00349-2

Products guided by the article

Product name:(S)-(+)-5-(4-carboxyphenyl)-5-methylhydantoin

Cas No:197229-09-7

R&D Labs maybe for 197229-09-7

SHIJIAZHUANG HENRYTE CHEMICALS CO,.LTD(expird)

Contact:+86-311-85208698 311-80837698

Address:NO.166, yuhua west road, SHIJIAZHUANG, China
Langchem

Contact:+86+21-58956006 15800617331

Address:402 Room, 150# Cailun Road, Zhangjiang high tech park, Shanghai
Hubei anhuang chemical Co.Ltd

Contact:

Address:308# dongwu avenue dongxihu district wuhan city
Hangzhou Yingshanhua Pigment Chemicals Co.,Ltd.

Contact:+86-0150-58101658

Address:Nanyang Economic DevelopmentZong,Xiaoshan,Hangzhou,China
ZHANGJIAGANG FREE TRADE ZONE YONG HAN INTERNATIONAL TRADING CO., LTD(expird)

Contact:86 512 57910558

Address:qianjin M road

Relevant to this article

Structure-activity relationship of a series of C-terminus modified aminoalkyl, diaminoalkyl- and anilino-containing analogues of the benzoic acid mustard distamycin derivative tallimustine: Synthesis, DNA binding and cytotoxicity studies

Doi:10.1016/S0968-0896(97)00096-5
(1997)
Acid-base control of a migratory insertion reaction: p-Aminophenyl derivatives of ruthenium(II) and the crystal structure of Ru(η²-C[O]C₆H₄NH ₂-4)Cl(CO)(PPh₃)₂

Doi:10.1021/om970714r
(1997)
A novel, chemically robust, amine releasing linker

Doi:10.1016/S0040-4039(97)01627-4
(1997)
An efficient method for the preparation of optically active 4-hydroxy-Δ²-isoxazolines

Doi:10.1016/S0040-4039(97)01596-7
(1997)
Nucleophilic Alkylation on Anti-Bredt Iminium Ions. Facile Entry to the Synthesis of 1-Alkylated 2-Azabicyclo[3.3.1]nonanes (Morphans) and 5-Azatricyclo[6.3.1.0^1,5]dodecane

Doi:10.1021/jo9715579
(1997)
New 2-Pyrazoline and Hydrazone Derivatives as Potent and Selective Monoamine Oxidase A Inhibitors

Doi:10.1021/acs.jmedchem.0c01504
(2021)

Article Doi