1-Cbz-pyrrolidine

General

Type : Epoxide || Benzyloxycarbonyl || Carbamate

Chemical_Nomenclature : benzyl pyrrolidine-1-carboxylate

Canonical SMILES : C1CCN(C1)C(=O)OCC2=CC=CC=C2

InChI : InChI=1S\/C12H15NO2\/c14-12(13-8-4-5-9-13)15-10-11-6-2-1-3-7-11\/h1-3,6-7H,4-5,8-10H2

InChIKey : VALPXRNQZYGXPS-UHFFFAOYSA-N

Other name(s) : N-benzyloxycarbonyl-3,4-epoxy-pyrrolidine,     Benzyl Pyrrolidine-1-carboxylate,     1-Pyrrolidinecarboxylic acid, phenylmethyl ester,     MFCD18206031,     SCHEMBL1000788


MW : 205.25

Formula : C12H15NO2

CAS_number : 25070-74-0

PubChem :

UniChem :

Iuphar :

Target

Families : Epoxide_hydrolase

References (2)

Title : Enantioselective Hydrolysis of Racemic and Meso-Epoxides with Recombinant Escherichia coli Expressing Epoxide Hydrolase from Sphingomonas sp. HXN-200: Preparation of Epoxides and Vicinal Diols in High ee and High Concentration - Wu_2013_ACS.Catal_3_752
Author(s) : Wu S , Li A , Chin YS , Li Z
Ref : ACS Catal , 3 :752 , 2013
Abstract : Wu_2013_ACS.Catal_3_752
ESTHER : Wu_2013_ACS.Catal_3_752
PubMedSearch : Wu_2013_ACS.Catal_3_752
PubMedID:
Gene_locus related to this paper: 9sphn-a0a191xv39

Title : Highly enantioselective hydrolysis of alicyclic meso-epoxides with a bacterial epoxide hydrolase from Sphingomonas sp. HXN-200: simple syntheses of alicyclic vicinal trans-diols - Chang_2003_Chem.Commun.(Camb)__960
Author(s) : Chang D , Wang Z , Heringa MF , Wirthner R , Witholt B , Li Z
Ref : Chem Commun (Camb) , :960 , 2003
Abstract : Chang_2003_Chem.Commun.(Camb)__960
ESTHER : Chang_2003_Chem.Commun.(Camb)__960
PubMedSearch : Chang_2003_Chem.Commun.(Camb)__960
PubMedID: 12744319
Gene_locus related to this paper: 9sphn-a0a191xv39