Catalyst-free one-pot domino reactions for selective synthesis of functionalized 2,8-oxazabicyclo[3.3.1]-nonanes and 5H-indeno[1,2-b]pyridin-5-ones-Reference-Cited by-同舟云学术

Catalyst-free one-pot domino reactions for selective synthesis of functionalized 2,8-oxazabicyclo[3.3.1]-nonanes and 5H-indeno[1,2-b]pyridin-5-ones

Published:2014 Issue:110 Volume:4 Page:64551-64558
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Rao Yin¹²³⁴,Liu Meilin¹²³⁴,Wu Lu¹²³⁴,Yin Guodong¹²³⁴

Affiliation:

1. Hubei Collaborative Innovation Center for Rare Metal Chemistry

2. Hubei Key Laboratory of Pollutant Analysis and Reuse Technology

3. Hubei Normal University

4. Huangshi 435002, China

Abstract

A simple and efficient method for one-pot selective synthesis of functionalized 2,8-oxazaxabicyclo[3.3.1]nonanes and hydroxy-containing 5H-indeno[1,2-b]pyridin-5-ones under catalyst-free conditions has been developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA13166E

Reference69 articles.

1. Syntheses and Applications of Functionalized Bicyclo[3.2.1]octanes: Thirteen Years of Progress

2. Domino reactions for the synthesis of bridged bicyclic frameworks: fast access to bicyclo[n.3.1]alkanes

3. Novel Syntheses of Bridge-Containing Organic Compounds

4. Synthesis and Self-Aggregation of Enantiopure and Racemic Molecular Tweezers Based on the Bicyclo[3.3.1]nonane Framework

5. Congeners of Troeger's base as chiral ligands

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