Literature DB >> 3572975

Structure-activity relationships in the 2-arylcarbapenem series: synthesis of 1-methyl-2-arylcarbapenems.

R N Guthikonda, L D Cama, M Quesada, M F Woods, T N Salzmann, B G Christensen.   

Abstract

The labile tert-butyldimethylsilyl esters of the azetidinones 6-8b served as the crucial synthons in the preparation of the potentially useful ylide pyridyl thio esters 18-20. These intermediates were utilized to synthesize a host of title carbapenems 25-30d, 32, and 49-53. The antimicrobial properties and DHP-I susceptibility of these carbapenems were studied with reference to thienamycin.

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Year:  1987        PMID: 3572975     DOI: 10.1021/jm00388a022

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  3 in total

1.  Pharmacokinetics of the penem CP-65,207 and its separate stereoisomers in humans.

Authors:  G Foulds; A K Knirsch; J D Lazar; T G Tensfelt; N Gerber
Journal:  Antimicrob Agents Chemother       Date:  1991-04       Impact factor: 5.191

2.  Expeditious synthesis of cis-1-methyl-2, 3,3a,4,5,9b-hexahydro-1H-pyrrolo-[3,2h]isoquinoline / [2,3-f]quinoline via azomethine ylide-alkene [3+2] cycloaddition.

Authors:  Zhenfa Zhang; Linda P Dwoskin; Peter A Crooks
Journal:  Tetrahedron Lett       Date:  2011-05-25       Impact factor: 2.415

3.  Toward a synthesis of hirsutellone B by the concept of double cyclization.

Authors:  Keith P Reber; S David Tilley; Cheryl A Carson; Erik J Sorensen
Journal:  J Org Chem       Date:  2013-09-23       Impact factor: 4.354

  3 in total

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