N-acyliminium ion cyclisations in natural product chemistry: Synthesis of gelsemine-Reference-Cited by-同舟云学术

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N-acyliminium ion cyclisations in natural product chemistry: Synthesis of gelsemine

Published:1994-01-01 Issue:10-11 Volume:66 Page:2163-2166
ISSN:1365-3075
Container-title:Pure and Applied Chemistry
language:
Short-container-title:

Author:

Speckamp W. N.,Newcombe N. J.,Hiemstra Henk,Ya Fang,Vijn R. J.,Koot W.-J.

Publisher

Walter de Gruyter GmbH

Subject

General Chemical Engineering,General Chemistry

Link

https://www.degruyter.com/document/doi/10.1351/pac199466102163/pdf

Reference2 articles.

1. cited therein a For recent studies in this area see a;Lin;Tetrahedron Lert Tetrahedron Lert Tetrahedron Lett Heterocycles Chem SOC Perkin Trans Tetrahedron Org Chem Tefruhedron Lett Prod Rep,1991

2. a;Hiemstra;Org Chem Chem,1987

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1. Total Synthesis of Gelsemoxonine;Journal of the American Chemical Society;2011-10-13

2. Transition‐Metal‐Mediated Routes to 3,3‐Disubstituted Oxindoles through Anilide Cyclisation;European Journal of Organic Chemistry;2011-09-23

3. Molecular Complexity via C–H Activation: A Dehydrogenative Diels–Alder Reaction;Journal of the American Chemical Society;2011-09-01

4. ChemInform Abstract: N-Acyliminium Ion Cyclizations in Natural Product Chemistry: Synthesis of Gelsemine.;ChemInform;2010-08-18

5. A facile synthesis of 5-alkoxypyrrol-2(5H)-ones using a modified aza-Achmatowicz oxidation;Tetrahedron;2009-08

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