Conversion of indoles into quinolines through the n-1-c-2 fission by singlet-oxygen as a model experiment of biomimetic synthesis of quinine alkaloids-Reference-Cited by-同舟云学术

Conversion of indoles into quinolines through the n-1-c-2 fission by singlet-oxygen as a model experiment of biomimetic synthesis of quinine alkaloids

Published:1985-01 Issue:11 Volume:41 Page:2109-2114
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Ihara Masataka,Noguchi Kazuharu,Fukumoto Keiichiro,Kametani Tetsuji

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

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1. Streptonigrin biosynthesis. 3. Determination of the primary precursors to the 4-phenylpicolinic acid portion

2. Streptonigrin biosynthesis. 4. Details of the tryptophan metabolism

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4. Biosynthesis of the Cinchona alkaloids: late stages of the pathway

5. Biosynthesis of camptothecin. 3. Definition of strictosamide as the penultimate biosynthetic precursor assisted by carbon-13 and deuterium NMR spectroscopy

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