Synthesis of the naturally occurring 6-(3-methylbuta-1,3-dienyl)indole via advanced fischer indolization of a 2-methoxyphenylhydrazone derivative
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference4 articles.
1. 6-(3-Methylbuta-1,3-dienyl)indole from Monodora tenuifolia
2. Development of "Abnormal" Fischer Indolization to Syntheses of 3, 6'-Biindole and Its Derivatives
3. A route to aldehydes and ketones by a four-electron decarboxylative oxidation utilizing pyridine N-oxide
4. Eine neue reaktion von pyridin-N-oxyd mit säureanhydriden
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. SmI2-mediated dimerization of indolylbutenones and synthesis of the myxobacterial natural product indiacen B;Beilstein Journal of Organic Chemistry;2015-09-21
2. Peculiarity of methoxy group-substituted phenylhydrazones in Fischer indole synthesis;Proceedings of the Japan Academy, Series B;2012
3. The phytochemistry of the annonaceae;Phytochemistry;1980-01
4. ChemInform Abstract: SYNTH. VON NATUERLICH VORKOMMENDEM 6-(3-METHYLBUTA-1,3-DIENYL)-INDOL UEBER EINE FISCHER-INDOLISIERUNG EINES 2-METHOXYPHENYL-HYDRAZON-DERIVATS;Chemischer Informationsdienst;1973-04-17
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