Acyclic stereochemical control using hexacarbonyldicobalt stabilized propargyl cation. A highly stereoselective route to 1β-methylcarbapenem precursors.-Reference-Cited by-同舟云学术

Acyclic stereochemical control using hexacarbonyldicobalt stabilized propargyl cation. A highly stereoselective route to 1β-methylcarbapenem precursors.

Published:1987-01 Issue:17 Volume:28 Page:1857-1860
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Rrasad J.Siva,Liebeskind Lanny S.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference25 articles.

1. The Chemistry of Thienamycin and Other Carbapenem Antibiotics;Ratcliffe,1982

2. Synthesis of Carbapenem Antibiotics

3. Synthetic Carbapenem Antibiotics. I. 1-b-Methylcarbapenem

4. Synthetic carbapenem antibiotics II. Stereoisomers of 7-hydroxyethyl-2,2,5-trimethyl-3-oxa-1-azabicyclo[4.2.O]octan-8-one

5. Synthetic carbapenem antibiotics III. 1-Methyl thienamycin

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