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Dive into the research topics where David Mack Floyd is active.

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Enfermedades Infecciosas Y Microbiologia Clinica | 1985

Beta-lactam antibiotics

Richard B. Sykes; William Lawrence Parker; Christopher Michael Cimarusti; William Henry Koster; William Allen Slusarchyk; Alan William Fritz; David Mack Floyd

Beta-lactam drugs, whose mechanism of action is inhibition of the last stage of bacterial cell wall synthesis, are the largest family of antimicrobial agents and the most widely used in current clinical practice. These drugs have a slow, time-dependent bactericidal action, generally good distribution in the body, and low toxicity. Modifications of the original molecule have led to new compounds with a greater antimicrobial spectrum and activity; nonetheless, the use and efficacy of beta-lactams is limited in some clinical settings, owing to the increasing emergence of antimicrobial resistance. Despite this problem, penicillin remains the treatment of choice in a large number of infections, cephalosporins have a wide range of indications, carbapenems are used in nosocomially-acquired infection and infection caused by multiresistant microorganisms, and beta-lactam inhibitors restore the spectrum of activity of their companion penicillins (aminopenicillins, ureidopenicillins) when resistance is caused by beta lactamase production.


Journal of the American Chemical Society | 1981

Chemistry of higher order, mixed organocuprates. 1. Substitution reactions at unactivated secondary centers

Bruce H. Lipshutz; Robert S. Wilhelm; David Mack Floyd


Journal of Organic Chemistry | 1978

(3-Methyl-3-methoxy-1-butynyl)copper, a useful reagent for the generation of mixed cuprates

E. J. Corey; David Mack Floyd; Bruce H. Lipshutz


ChemInform | 2002

Total synthesis of (-)-N-methylmaysenine

E. J. Corey; Leland O. Weigel; David Mack Floyd; Mark G. Bock


Journal of Organic Chemistry | 1982

Monobactams. Stereospecific synthesis of (S)-3-amino-2-oxoazetidine-1-sulfonic acids

David Mack Floyd; Alan William Fritz; Christopher M. Cimarusti


Tetrahedron Letters | 1978

A key intermediate for the synthesis of maytansine and related antitumor agents

E. J. Corey; Mark G. Bock; Alan P. Kozikowski; A. V. Rama Rao; David Mack Floyd; Bruce Lipshutz


Journal of Organic Chemistry | 1972

11,15-Epiprostaglandin E 2 and its enantiomer. Biological activity and synthesis.

E. J. Corey; Shiro. Terashima; Peter W. Ramwell; Reginald. Jessup; Ned M. Weinshenker; David Mack Floyd; Guy A. Crosby


Journal of Organic Chemistry | 1982

Monobactams. The conversion of 6-APA to (S)-3-amino-2-oxoazetidine-1-sulfonic acid and its 3 (RS)-methoxy derivative

Christopher M. Cimarusti; Harold E. Applegate; H. W. Chang; David Mack Floyd; W. H. Koster; W. A. Slusarchyk; M. G. Young


The Journal of Antibiotics | 1982

SQ 26,180, a novel monobactam. II Isolation, structure determination and synthesis.

William L. Parker; William Henry Koster; Christopher M. Cimarusti; David Mack Floyd; Wen-Chih Liu; Marlene L. Rathnum


ChemInform | 1983

MONOBACTAMS. PREPARATION OF (S)-3-AMINO-2-OXOAZETIDINE-1-SULFONIC ACIDS FROM L-α-AMINO-β-HYDROXY ACIDS VIA THEIR HYDROXAMIC ESTERS

David Mack Floyd; A. W. Fritz; J. Pluscec; E. R. Weaver; Christopher M. Cimarusti

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