Chemical investigation of L. tongolensis afforded two new eremophilenolides, which were identified as 3β-（2＇-methylbutanoyloxy）-8βH-eremophil-7（11）-en-12, 8α（14, 6α）-diolide （1）and 8βH-eremophil-3, 7（11...Chemical investigation of L. tongolensis afforded two new eremophilenolides, which were identified as 3β-（2＇-methylbutanoyloxy）-8βH-eremophil-7（11）-en-12, 8α（14, 6α）-diolide （1）and 8βH-eremophil-3, 7（11）-dien-12, 8α （14, 6α）-diolide （2）. Their structures were established by spectroscopic methods including 2D NMR experiments.展开更多
Chemical investigation of L. fischeri afforded two new eremophilenolides. which were identified as 6 beta-methoxy-8 beta-hpdroxy-eremophil-7(11)-en-12,8 alpha-olide 1; 6-oxo-8 beta-hydroxy-eremophil-7(11)-en- 12.8 alp...Chemical investigation of L. fischeri afforded two new eremophilenolides. which were identified as 6 beta-methoxy-8 beta-hpdroxy-eremophil-7(11)-en-12,8 alpha-olide 1; 6-oxo-8 beta-hydroxy-eremophil-7(11)-en- 12.8 alpha-olide 2.展开更多
Chemical investigation of L.sagitta afforded two new cremophilenolides, which were identified as 6beta-angeloyloxy-10beta-hydroxy-8beta-methoxy-cremophil-7(11)-en-12, 8alpha-olide (1) and 6beta, 8beta-dimethoxy-10beta...Chemical investigation of L.sagitta afforded two new cremophilenolides, which were identified as 6beta-angeloyloxy-10beta-hydroxy-8beta-methoxy-cremophil-7(11)-en-12, 8alpha-olide (1) and 6beta, 8beta-dimethoxy-10beta-hydroxy-eremophil-7(11)-en-12, 8alpha-olide (2). Their structures were established by spectroscopic methods including 2D NMR experiments.展开更多
基金This work was supported by the NNSFC(No.20372029 and No,20021001)by the Key Project of Chinese Ministry of Education(No.104178).
文摘Chemical investigation of L. tongolensis afforded two new eremophilenolides, which were identified as 3β-（2＇-methylbutanoyloxy）-8βH-eremophil-7（11）-en-12, 8α（14, 6α）-diolide （1）and 8βH-eremophil-3, 7（11）-dien-12, 8α （14, 6α）-diolide （2）. Their structures were established by spectroscopic methods including 2D NMR experiments.
文摘Chemical investigation of L. fischeri afforded two new eremophilenolides. which were identified as 6 beta-methoxy-8 beta-hpdroxy-eremophil-7(11)-en-12,8 alpha-olide 1; 6-oxo-8 beta-hydroxy-eremophil-7(11)-en- 12.8 alpha-olide 2.
文摘Chemical investigation of L.sagitta afforded two new cremophilenolides, which were identified as 6beta-angeloyloxy-10beta-hydroxy-8beta-methoxy-cremophil-7(11)-en-12, 8alpha-olide (1) and 6beta, 8beta-dimethoxy-10beta-hydroxy-eremophil-7(11)-en-12, 8alpha-olide (2). Their structures were established by spectroscopic methods including 2D NMR experiments.
