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

Triumph International Development Limilted

website:http://www.jiashengchem.cn/

Contact:+86-536-7971999

Address:Yinhai Road,Shouguang
Taiwan Surfactant Corp.

Contact:886 2 2541 0022

Address:8 Fl., No. 11, Sec. 1, Chung Shan North Rd., Taipei, Taiwan R.O.C.
Shanghai ZaiQi Bio-Tech Co., Ltd.,

Contact:+86-21-5482 4098

Address:Bldg. No.7, No.201 MinYi Rd，Songjiang CaoHeJing High-Tech Park Shanghai 201516 P,R,China
KA-SHING Business Trade Macau Co., Ltd.

Contact:00853-28430045

Address:23rd Floor, Block 3 La Cite, Areia Preta, Macao
MENGNA

Contact:18698110882

Address:1303 No2 building,LuoMa Garden,YongAn Road,Hexi District,Tianjin city

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