Efficient Transformation of Alkyl 3-nitro-5-(aryl/alkyl)isoxazole-4-carboxylates into 3-amino- and 3-hydrazinyl-5-aryl/alkyl-isoxazole-4-carboxylates in Aqueous Solution-Reference-Cited by-同舟云学术

Efficient Transformation of Alkyl 3-nitro-5-(aryl/alkyl)isoxazole-4-carboxylates into 3-amino- and 3-hydrazinyl-5-aryl/alkyl-isoxazole-4-carboxylates in Aqueous Solution

Published:2017-09-29 Issue:22 Volume:359 Page:4050-4056
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Mukhopadhyay Sushobhan¹,Barak Dinesh S.¹,Avasthi Ilesha²,Batra Sanjay¹³

Affiliation:

1. Medicinal and Process Chemistry Division; CSIR-Central Drug Research Institute; Sector 10, Jankipuram Extension, Sitapur Road Lucknow 226031 India

2. Indian Institute of Technology; Kanpur, Kanpur 208016 India

3. Academy of Scientific and Innovative Research; New Delhi- 110025 India

Funder

Indian Institute of Technology

Publisher

Wiley

Subject

General Chemistry

Reference24 articles.

1. Identification of 1-(3-(6,7-Dimethoxyquinazolin-4-yloxy)phenyl)-3-(5-(1,1,1-trifluoro-2-methylpropan-2-yl)isoxazol-3-yl)urea Hydrochloride (CEP-32496), a Highly Potent and Orally Efficacious Inhibitor of V-RAF Murine Sarcoma Viral Oncogene Homologue B1 (BRAF) V600E

2. Dual Angiotensin II and Endothelin A Receptor Antagonists: Synthesis of 2‘-Substituted N-3-Isoxazolyl Biphenylsulfonamides with Improved Potency and Pharmacokinetics

3. The Discovery of Sulfonamide Endothelin Antagonists and the Development of the Orally Active ETA Antagonist 5-(Dimethylamino)-N-(3,4-dimethyl-5- isoxazolyl)-1-naphthalenesulfonamide

4. Discovery and optimization of a highly efficacious class of 5-aryl-2-aminopyridines as FMS-like tyrosine kinase 3 (FLT3) inhibitors

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