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首页> 外文期刊>Tetrahedron >Biosynthesis of naphthylisoquinoline alkaloids: synthesis and incorporation of an advanced C-13(2)-labeled isoquinoline precursor
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Biosynthesis of naphthylisoquinoline alkaloids: synthesis and incorporation of an advanced C-13(2)-labeled isoquinoline precursor

机译:萘基异喹啉生物碱的生物合成:先进的C-13(2)标记的异喹啉前体的合成和掺入

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摘要

Biosynthetic studies on naphthylisoquinoline alkaloids involving a specifically [1,1,-13 C-2]-labeled dihydroisoquinoline 7 are described. The synthesized precursor 7 was fed to callus cultures of Triphyophyllum peltatum and the isolated secondary metabolites were characterized by spectroscopic methods (H-1, C-13 NMR, and INADEQUATE experiments). The unambiguous incorporation of the precursor into dioncophylline A and two minor naphthylisoquinolines, together with the formation of the labeled corresponding trans-configured tetrahydroisoquinoline, proves the implication of such advanced intermediates in the proposed biosynthetic pathway of naphthylisoquinoline alkaloids. (c) 2006 Elsevier Ltd. All rights reserved.
机译:描述了涉及萘基异喹啉生物碱的生物合成研究,该生物碱特别被[1,1,-13 C-2]标记的二氢异喹啉7涉及。将合成的前体7喂入白粉菌的愈伤组织培养物中,并通过光谱方法(H-1,C-13 NMR和INADEQUATE实验)对分离的次级代谢产物进行表征。前体毫不含糊地并入二药茶碱A和两个较小的萘基异喹啉中,并形成了标记的相应反式构型四氢异喹啉,证明了这种高级中间体对萘基异喹啉生物碱的拟议生物合成途径有影响。 (c)2006 Elsevier Ltd.保留所有权利。

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