Substrate specificity of proline 4-hydroxylase: Chemical and enzymatic synthesis of 2S,3R,4S-epoxyproline

DOI: 10.1016/S0040-4039(00)60753-0

Source and publish data:

Tetrahedron Letters p. 4649 - 4652 (1994)

Update date:2022-08-05

Topics:

Authors:

Baldwin Baldwin

Field Field

Lawrence

Lee Lee

Robinson

Schofield

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

Article abstract of DOI:10.1016/S0040-4039(00)60753-0

The substrate specificity of L-proline 4-hydroxylase, a 2-oxoglutarate dependent dioxygenase from Streptomyces griseoviridus P8648, was investigated. Preliminary assays measuring turnover of 2-oxyglutarate indicated 3,4-dehydro-L-proline was an efficient

Full text of DOI:10.1016/S0040-4039(00)60753-0

Products guided by the article

Product name:dibenzyl (2S,4S)-4-(phenylselanyl)pyrrolidine-1,2-dicarboxylate

Cas No:159551-88-9

R&D Labs maybe for 159551-88-9

Jiangxi Huashi Pharmaceutical Co., Ltd

Contact:+86-795-4509628

Address:No.199, Ningbo Avenue, Fengxin industrial park, Fengxin county, Yichun city, Jiangxi
MS( MAOSHENG )Chemical CO.,LTD

Contact:+86-519-82726678.82726378

Address:TAOXI INDUSTRY ZONE JINTAN
Landz International Company Ltd.

Contact:0086-21-58891610

Address:985 Dongfang Road, Pudong, Shanghai 200122 China
Angel Yeast Co., Ltd.

Contact:+86-717-6370352

Address:168 Chengdong Avenue, Yichang, Hubei 443003, P. R.China
Shandong Topscience Biotech Co., Ltd.

Contact:0633-2619278

Address:No. 98 Lanshan West Road, Lanshan District, Rizhao, Shandong Province, P.R. of China

Relevant to this article

Facile synthesis, X-ray analysis, and spectroscopic studies of di-iron propanedithiolate complexes with tris(aromatic)phosphine ligands

Doi:10.1080/00958972.2014.903329
(2014)
Synthesis of 3-amino-3-hydroxymethyloxindoles and 3-hydroxy-3- hydroxymethyloxindoles by Rh₂(OAc)₄-catalyzed three-component reactions of 3-diazooxindoles with formaldehyde and anilines or water

Doi:10.1021/jo500307n
(2014)
From (S)-α-Amino β-Hydroxyacids To (R)-α,β-Diamino-γ-Hydroxyacid N-Carboxyanhydrides via β-Lactams

Doi:10.1016/S0040-4039(00)77016-X
(1994)
Novel thiazole-based heterocycles as selective inhibitors of fibrinogen- mediated platelet aggregation

Doi:10.1021/jm00001a008
(1995)
Rh(NHC)-catalyzed direct and selective arylation of quinolines at the 8-position

Doi:10.1021/ja111670s
(2011)
Gold-catalysed cyclisation of N-propargylic β-enaminones to form 3-methylene-1-pyrroline derivatives

Doi:10.1039/c3ob42513d
(2014)

Article Doi