2000
DOI: 10.1016/s0031-9422(99)00434-3
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Cassane diterpenoid from Caesalpinia major

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Cited by 21 publications
(14 citation statements)
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“…DANDY et EXELL (also under the name of its synonymous name C. bonducella), [5][6][7][8][9] and C. pulcherrima (L.) SWARTZ [10][11][12][13][14][15] of medicinal value among the genus, which revealed the presence of characteristic furano-diterpenes phytochemically classified as cassane diterpenes and otherwise known as caesalpins. We also undertook chemical studies on C. bonduc seeds that have been reputed in both Indonesian and Philippine traditional medicine, and reported the isolation of a new type of hemiacetal diterpenes fused with an a,b-butenolide ring for which the general skeletal name of neocaesalpins was proposed.…”
Section: )mentioning
confidence: 99%
“…DANDY et EXELL (also under the name of its synonymous name C. bonducella), [5][6][7][8][9] and C. pulcherrima (L.) SWARTZ [10][11][12][13][14][15] of medicinal value among the genus, which revealed the presence of characteristic furano-diterpenes phytochemically classified as cassane diterpenes and otherwise known as caesalpins. We also undertook chemical studies on C. bonduc seeds that have been reputed in both Indonesian and Philippine traditional medicine, and reported the isolation of a new type of hemiacetal diterpenes fused with an a,b-butenolide ring for which the general skeletal name of neocaesalpins was proposed.…”
Section: )mentioning
confidence: 99%
“…Caesalpinia sp. has a propensity for producing cassane furanoditerpenes (Kinoshita et al, 2005;Kaluni et al, 2005;Lyder et al, 1998a;Jiang et al, 2001;Linn et al, 2005;Ragasa et al, 2002;Jiang et al, 2002;Roengsumran et al, 1998). Among cassane diterpenes production of the cassane butenolides or butenolide hemiketals is possibly via photooxygenation of the furan ring and these compounds have very limited distribution (Lyder et al, 1998b;Torres-Mendoza et al, 2004;Roach et al, 2003;Kinoshita et al, 2005;Jiang et al, 2002).…”
Section: Introductionmentioning
confidence: 99%
“…Theses diterpenoids can be classified into eight categories: caesalpin, e.g., 14-deoxy-e-caesalpin [1]; neocaesalpin, e.g., neocaesalpin H [2]; caesaldekarin, e.g., caesaldekarin G [3]; caesalpinin, e.g., caesalpinin H [4]; caesalmin, e.g., caesalmin A [5]; bonducellin, e.g., bonducellpin D [6]; norcaesalpinin, e.g., norcaesalpinin F [4], and macrocaesalmin [4]. -The genus Caesalpinia is a rich source of cassane diterpenoids.…”
mentioning
confidence: 99%
“…Phytochemical studies on the seed of Caesalpinia minax Hance have led to the isolation of five new cassane-diterpene-lactones, named neocaesalpin J -N (1)(2)(3)(4)(5)resp;Fig. 1), and together with nine known furanoditerpenoids, i.e., e-caesalpin, 7-acetoxy-ecaesalpin, 14-deoxy-e-caesalpin [1], caesalmin D -F [10], bonducellin C -D [6], and neocaesalpin A [11].…”
mentioning
confidence: 99%