Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade-Reference-Cited by-同舟云学术

Straightforward Access to the [3.2.2]Nonatriene Structural Framework via Intramolecular Cyclopropenation/Buchner Reaction/Cope Rearrangement Cascade

Published:2015-02-10 Issue:4 Volume:17 Page:790-793
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Xu Xinfang¹²,Wang Xiangbo¹,Zavalij Peter Y.²,Doyle Michael P.²

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China

2. Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, United States

Funder

National Institute of General Medical Sciences

Division of Chemistry

Key Laboratory of Organic Synthesis of Jiangsu Province

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol503498n

Reference45 articles.

1. Ueber die Einwirkung von Diazoessigäther auf aromatische Kohlenwasserstoffe

2. THE STRUCTURE OF THE BUCHNER ACIDS

3. Asymmetric Synthesis of Deoxypolypropionate Units via Stereoselective Hydrogenation of Optically Active Cycloheptatriene

4. Pseudoguaianolides from intramolecular cycloadditions of aryl diazoketones: synthesis of (±)-confertin and an approach to the synthesis of (±)-damsin

5. α-Diazo-β-ketonitriles: Uniquely Reactive Substrates for Arene and Alkene Cyclopropanation

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