Preparation of new heterocyclic compounds characterised by 1,3-imidazolidine structure useful for stereoselective synthesis of optically pure key intermediates in methylcarbapenem production

Process for preparation of 1,3-imidazolidine derivatives as intermediates for synthesizing carbapenem

FRECCERO, MAURO;
2010-01-01

Abstract

Preparation of new heterocyclic compounds characterised by 1,3-imidazolidine structure useful for stereoselective synthesis of optically pure key intermediates in methylcarbapenem production
2010
6-mag-2010
The Organic Chemistry/Polymer Science category includes resources concerned with the related fields of organic chemistry and polymer science. The organic chemistry resources deal with compounds of carbon with the exception of certain simple ones, such as the carbon oxides, carbonates, cyanides and cyanates (see Inorganic & Nuclear Chemistry). This category includes research on synthetic and natural organic compounds that may include other elements, such as hydrogen and oxygen, but also nitrogen, halogens, sulphur and phosphorous. Resources concerned with hydrocarbons, organic compounds containing only the elements carbon and hydrogen, are also included in this category. Examples are the alkanes, alkenes, alkynes and aromatics, such as benzene and naphthalene. Polymer science includes all resources dealing with the study, production and technology of polymers, which are compounds composed of very large molecules made up of repeating molecular units (monomers). Polymers may be natural substances, such as polysaccharides or proteins, or synthetic materials, such as nylon or polyethylene.
WO 2010049233
ACS Dobfar S.p.A., Italy
ELETTRONICO
Inglese
Internazionale
Stereoselective synthesis; carbapenem; Reformatsky reaction
http://v3.espacenet.com/publicationDetails/biblio?DB=EPODOC&adjacent=true&locale=en_ep&FT=D&date=20100506&CC=WO&NR=2010049233A1&KC=A1
6 Brevetti::6.1 Brevetto
none
Freccero, Mauro; Fogliato, Giovanni; Manca, Antonio; Bassanini, Michele
info:eu-repo/semantics/patent
285
4
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/218463
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