1989ChemInformRequires access

ChemInform Abstract: Synthesis of 3‐(Alkyl and Aryl)thio‐2‐isocephems.

József Aszódi, Jean‐François Chantot, Jeannine Collard, Georges Teutsch

Open publisher page 0 citations

Abstract

Abstract Coupling reaction of the aromatic sulfenyl chlorides (II) with the diazopyruvate (III) followed by cyclization with the mercaptomethylazetidinone (I) yields the isocephamcarboxylates (IV) which are dehydrated and deprotected to give the isocephemcarboxylic acids (VI).

About this research paper

What this paper is about

Abstract Coupling reaction of the aromatic sulfenyl chlorides (II) with the diazopyruvate (III) followed by cyclization with the mercaptomethylazetidinone (I) yields the isocephamcarboxylates (IV) which are dehydrated and deprotected to give the isocephemcarboxylic acids (VI).

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Abstract Coupling reaction of the aromatic sulfenyl chlorides (II) with the diazopyruvate (III) followed by cyclization with the mercaptomethylazetidinone (I) yields the isocephamcarboxylates (IV) which are dehydrated and deprotected to give the isocephemcarboxylic acids (VI).

Key concepts: Chemistry, Thio-, Aryl, Alkyl, Medicinal chemistry, Organic chemistry, Combinatorial chemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
ChemInform Abstract: Synthesis of 3‐(Alkyl and Aryl)thio‐2‐isocephems. — Research Paper | ScholarLens