Method for Accessing Nitrogen-Containing, B-Heteroaryl-Substituted 2,1-Borazaronaphthalenes-Reference-Cited by-同舟云学术

Method for Accessing Nitrogen-Containing, B-Heteroaryl-Substituted 2,1-Borazaronaphthalenes

Published:2016-12-14 Issue:1 Volume:82 Page:549-555
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Davies Geraint H. M.¹,Zhou Zhao-Zhao¹²,Jouffroy Matthieu¹,Molander Gary A.¹^ORCID

Affiliation:

1. Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104-6323, United States

2. State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, P.R. China

Funder

China Scholarship Council

National Institute of General Medical Sciences

Eli Lilly and Company

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b02574

Reference23 articles.

1. Bioisosterism: A Rational Approach in Drug Design

2. Synopsis of Some Recent Tactical Application of Bioisosteres in Drug Design

3. Development of Thiophenic Analogues of Benzothiadiazine Dioxides as New Powerful Potentiators of 2-Amino-3-(3-hydroxy-5-methylisoxazol-4-yl)propionic Acid (AMPA) Receptors

4. 1,4,2-Benzo/pyridodithiazine 1,1-Dioxides Structurally Related to the ATP-Sensitive Potassium Channel Openers 1,2,4-Benzo/pyridothiadiazine 1,1-Dioxides Exert a Myorelaxant Activity Linked to a Distinct Mechanism of Action

5. B-N as a C-C substitute in aromatic systems

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