A NEW SYNTHETIC EQUIVALENT OF THE GLUTAMIC ACID γ-ANION AND ITS APPLICATION TO THE SYNTHESIS OF S-(+)-γ-CARBOXYGLUTAMIC ACID

DOI: 10.1016/S0040-4039(00)94393-4

Source and publish data:

Tetrahedron Letters p. 283 - 284 (1990)

Update date:2022-09-26

Topics:

Authors:

Attwood, Michael R.

Carr, Maria G.

Jordan, Steven

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

Article abstract of DOI:10.1016/S0040-4039(00)94393-4

Protected S-pyroglutamic acid can be deprotonated specifically at the γ-position.The resulting enolate can be converted into γ-carboxyglutamic acid in optically pure form.

Full text of DOI:10.1016/S0040-4039(00)94393-4

Products guided by the article

Product name:(2S)-1-tert-butyloxycarbonyl-4-benzyloxycarbonyl-5-oxoproline tert-butyl ester

Cas No:108732-30-5

R&D Labs maybe for 108732-30-5

Jiangxi Biochem Co.,Ltd

Contact:86-791-86629460

Address:1-6F, 118 Xinzhou road, Nanchang, Jiangxi, China
Yurui(Shanghai)Chemical Co.,Ltd

Contact:0086 21-50456736

Address:No.3188 Xiupu Road,Shanghai
Shanghai Dianyang Industry Co.,ltd

Contact:+86 21 6492 4669

Address:Chejing RD, Songjiang District, Shanghai, China
Shenzhen Hongyuan Import & Export Co., Ltd.

Contact:0755-26407171

Address:Shenzhen Hongyuan Chemical New Materials Technology Co., Ltd.
Anhui Hope-Chem Co., Ltd.

Contact:86-551-63540590

Address:No 1388 Furong Rd., Hefei, Anhui, China

Relevant to this article

Doi:10.1021/ja01600a054
(1956)
Phenacyl-Directed Alkylation of Imidazoles: A New Regiospecific Synthesis of 3-Substituted L-Histidines

Doi:10.1021/jo00392a018
(1987)
Synthesis of the Tridentate Pyridine Donor 2,6-Bis<1-phenyl-1-(pyridin-2-yl)ethyl>pyridine (L), including Separation of meso and rac Diastereoisomers via Methylmercury(II) Derivatives, and an X-Ray Structural Study of NO3*2H2O

Doi:10.1039/DT9860002201
(1986)
Photocatalytic oxidative heterocyclization of semicarbazones: An efficient approach for the synthesis of 1,3,4-oxadiazoles

Doi:10.1055/s-0034-1380493
(2015)
Doi:10.1002/macp.1958.020260122
(1958)
Doi:10.1139/v59-286
(1959)

Article Doi