An efficient entry to 1,2-benzisoxazoles via 1,3-dipolar cycloaddition of in situ generated nitrile oxides and benzyne-Reference-Cited by-同舟云学术

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An efficient entry to 1,2-benzisoxazoles via 1,3-dipolar cycloaddition of in situ generated nitrile oxides and benzyne

Published:2010 Issue:11 Volume:8 Page:2537
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Spiteri Christian,Mason Christopher,Zhang Fengzhi,Ritson Dougal J.,Sharma Pallavi,Keeling Steve,Moses John E.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2010/OB/B927235F

Reference47 articles.

1. CLINICAL THERAPEUTIC CONFERENCE

2. Zonisamide has beneficial effects on Parkinson's disease patients

3. Design and Synthesis of Aryl Diphenolic Azoles as Potent and Selective Estrogen Receptor-β Ligands

4. Zonisamide: chemistry, mechanism of action, and pharmacokinetics

5. New cholinesterase inhibitors: synthesis and structure-activity relationship studies of 1,2-benzisoxazole series and novel imidazolyl-d2-isoxazolines

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