67451-42-7Relevant articles and documents
Semisynthetic cephalosporins. Synthesis and structure-activity relationships of 7-(1-pyrryl)- and 7-(1-indolyl)acetamidocephalosporin derivatives
Nudelman,Karoly,Braun,Boehme,Erickson
, p. 962 - 964 (1978)
A series of 1-pyrrole- and 1-indoleacetamido derivatives of 3-heteroaryl-substituted cephalosporins was prepared. The most active compound in the series was 7[[2-(1-pyrryl)acetyl]amino]-3-[[(1- methyltetrazol-5-yl)thio]-methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0] oct-2-ene-2-carboxylic acid, which showed comparable potency in vitro and in vivo to that of cefazolin, and, in addition, was more potent than cefazolin against Enterobacter sp. and Providencia stuartii.
Azacycloalkanes: XXXIX. New Syntheses of 1H-Pyrrole-1-carboxylic acid and 1,2-dihydropyrrolo-[1,2-a]pyrazin-3(4H)-one derivatives
Mokrov,Likhosherstov,Troitskaya,Gudasheva
experimental part, p. 1829 - 1833 (2010/05/19)
New procedures have been developed for the synthesis of α-(2-formyl-1H-pyrrol-1-yl)-substituted carboxylic acids, α-(2-R-aminomethyl-1H-pyrrol-1-yl)-substituted carboxylic acids, and 1,2-dihydropyrrolo-[1,2-a]pyrazin-3(4H)-ones on the basis of furfurol and α-amino acids.
Improved functionalized resin for chemical synthesis
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, (2008/06/13)
A support functionalized by an indole or pyrrole aldehyde is useful for the solid phase synthesis of amide type compounds.