Arylspiroborates Derived from 4-tert-Butylcatechol and 3,5-Di-tert-butylcatechol and Their Antimicrobial Activities-Reference-Cited by-同舟云学术

Arylspiroborates Derived from 4-tert-Butylcatechol and 3,5-Di-tert-butylcatechol and Their Antimicrobial Activities

Published:2013-10-23 Issue:1 Volume:51 Page:157-161
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:J. Heterocyclic Chem.

Author:

Webb Michael I.¹,Halcovitch Nathan R.¹,Bowes Eric G.¹,Lee Graham M.¹,Geier Michael J.¹,Vogels Christopher M.¹,O'Neill Taryn²,Li Haoxin²,Flewelling Andrew²,Decken Andreas³,Gray Christopher A.²³,Westcott Stephen A.¹

Affiliation:

1. Department of Chemistry and Biochemistry; Mount Allison University; Sackville New Brunswick E4L 1G8 Canada

2. Department of Biology; University of New Brunswick; Saint John NB E2L 4L5 Canada

3. Department of Chemistry; University of New Brunswick; Fredericton New Brunswick E3B 5A3 Canada

Publisher

Wiley

Subject

Organic Chemistry

Reference31 articles.

1. Structural Features of Lithium Organoborates

2. Rationally designed, chiral Lewis acid for the asymmetric induction of some Diels-Alder reactions

3. Highly Regioselective Anti-Markovnikov Palladium-Borate-Catalyzed Methoxycarbonylation Reactions: Unprecedented Results for Aryl Olefins

4. New boron(III)-catalyzed amide and ester condensation reactions

5. Synthesis and Application of a Chiral Diborate

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