2006
DOI: 10.1016/j.tetlet.2005.11.036
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Synthesis of 8-R-9c-alkyl-1-aryl-2-benzyl-1-hydroxy-1,2,9b,9c-tetrahydro-5-oxa-2-aza-cyclopenta[2,3]cyclopropa[1,2-a]naphthalene-3,4-diones and reaction thereof with acetic anhydride

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Cited by 5 publications
(2 citation statements)
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“…Shchepin et al 98 2-benzyl-1-hydroxy-1,2,9b,9c-tetrahydro-5-oxa-2-aza-cyclopenta [2,3]cyclopropa[1,2-a] naphthalene-3,4-diones 106; the acylation of these compounds occurred via an unexpected rearrangement to give 4 -alkyl-5 -aryl-1 -benzyl-3,4,2 ,3 -tetrahydro-2,2 -dioxospiro[chroman-3,3 -pyrrol]-4-yl acetates 107 (Scheme 28).…”
Section: Scheme 27mentioning
confidence: 99%
“…Shchepin et al 98 2-benzyl-1-hydroxy-1,2,9b,9c-tetrahydro-5-oxa-2-aza-cyclopenta [2,3]cyclopropa[1,2-a] naphthalene-3,4-diones 106; the acylation of these compounds occurred via an unexpected rearrangement to give 4 -alkyl-5 -aryl-1 -benzyl-3,4,2 ,3 -tetrahydro-2,2 -dioxospiro[chroman-3,3 -pyrrol]-4-yl acetates 107 (Scheme 28).…”
Section: Scheme 27mentioning
confidence: 99%
“…So, the judicious use of antibacterial agent is an important approach in an attempt to control the emergence of bacterial resistance. In order to discover more potent inhibitors, we have successfully attempted a novel and green synthesis of benzothiazol-2-ylsulfanyl-chromenes through substitution of chromenes with 2-Benzothiazolethiol [15].…”
Section: Introductionmentioning
confidence: 99%