Lalitha N, Annapurna J, Iyengar D S, Bhalerao U T
Organic Division II, Indian Institute of Chemical Technology, Hyderabad.
Arzneimittelforschung. 1991 Aug;41(8):827-30.
The preparation and in vitro antibacterial activity of a novel series of gem-diphenyl-spiro-cyclopropano-oxazolones (cis-1,2,2,5-tetraphenyl 6-oxa-4-azaspiro[2.4]hept-4-en-7-one) are described. The overall activity of these compounds was higher than that of the 2-aryl(alkyl)4-ylidene-oxazol-5-ones (azlactones). The gem-diphenyl-spiro-cyclopropano-oxazolones 1-4 have emerged as the most potent derivatives when tested against bacteria.
描述了一系列新型偕二苯基-螺环丙基-恶唑酮(顺式-1,2,2,5-四苯基-6-氧杂-4-氮杂螺[2.4]庚-4-烯-7-酮)的制备及其体外抗菌活性。这些化合物的总体活性高于2-芳基(烷基)-4-亚烷基-恶唑-5-酮(氮杂内酯)。偕二苯基-螺环丙基-恶唑酮1-4在针对细菌进行测试时已成为最有效的衍生物。