Synthesis of 2-Alkylidenepyrrolidines and Pyrroles by Condensation of 1,3-Dicarbonyl Dianions with α-Azidoketones and Subsequent Intramolecular Staudinger−Aza-Wittig Reaction-Reference-Cited by-同舟云学术

Synthesis of 2-Alkylidenepyrrolidines and Pyrroles by Condensation of 1,3-Dicarbonyl Dianions with α-Azidoketones and Subsequent Intramolecular Staudinger−Aza-Wittig Reaction

Published:2006-05-23 Issue:13 Volume:71 Page:4965-4968
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Freifeld Ilia¹,Shojaei Heydar¹,Langer Peter¹

Affiliation:

1. Institut für Biochemie, Ernst-Moritz-Arndt Universität Greifswald, Soldmannstr. 16, 17487 Greifswald, Germany, Institut für Organische Chemie, Georg-August-Universität Göttingen, Tammannstr. 2, 37077 Göttingen, Germany, Institut für Chemie, Universität Rostock, Albert-Einstein-Str. 3a, 18059 Rostock, Germany, and Leibniz-Institut für Katalyse e. V. an der Universität Rostock, Albert-Einstein-Str. 29a, 18059 Rostock, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo060593h

Reference48 articles.

1. Routes to mitomycins. New syntheses of the 2,3,5,8-tetrahydro-5,8-dioxo-1H-pyrrolo[1,2-a]indole ring system. An efficient synthesis of 7-methoxymitosene

2. Total synthesis of a mitosene

3. Concise total syntheses of dl-camptothecin and related anticancer drugs

4. Heterocycle Formation through Aza-Annulation: Stereochemically Controlled Syntheses of (.+-.)-5-Epitashiromine and (.+-.)-Tashiromine

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