Phytochemistry

The biosynthetic pathway of crucifer phytoalexins and phytoanticipins: de novo incorporation of deuterated tryptophans and quasi-natural compounds

MSC Pedras, DP Okinyo-Owiti, K Thoms, AM Adio

Index: Pedras, M. Soledade C.; Okinyo-Owiti, Denis P.; Thoms, Ken; Adio, Adewale M. Phytochemistry, 2009 , vol. 70, # 9 p. 1129 - 1138

Full Text: HTML

Citation Number: 16

Abstract

Although several biosynthetic intermediates in pathways to cruciferous phytoalexins and phytoanticipins are common, questions regarding the introduction of substituents at N-1 of the indole moiety remain unanswered. Toward this end, we investigated the potential incorporations of several perdeuterated d-and l-1′-methoxytryptophans, d-and l- tryptophans and other indol-3-yl derivatives into pertinent phytoalexins and ...

Related Articles:

Iron-Catalyzed Synthesis of C2 Aryl-and N-Heteroaryl-Substituted Tetrahydropyrans

[Liu, Jinxian; Ma, Shengming Organic and Biomolecular Chemistry, 2013 , vol. 11, # 25 p. 4186 - 4193]

Three??Component Reactions of Aromatic Aldehydes and Two Different Nucleophiles and their Leaving Ability??Determined Downstream Conversions of the Products

[Reimann; Erdle Pharmazie, 2000 , vol. 55, # 12 p. 907 - 912]

Synthesis, crystal structure and evaluation of cancer inhibitory activity of 4-[indol-3-yl-methylene]-1H-pyrazol-5 (4H)-one derivatives

[Jing, Lingling; Wang, Liang; Zhao, Yinglan; Tan, Rui; Xing, Xiumei; Liu, Ting; Huang, Wencai; Luo, Youfu; Li, Zicheng Journal of Chemical Research, 2012 , vol. 36, # 12 p. 691 - 696]

Synthesis, crystal structure and evaluation of cancer inhibitory activity of 4-[indol-3-yl-methylene]-1H-pyrazol-5 (4H)-one derivatives

[Journal of Chemical Research, , vol. 36, # 12 p. 691 - 696]

More Articles...