Synthesis of thiazolo[3,2-a]pyridines from enaminoesters by tandem conjugate addition-cyclization
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Nifedipine A Review of Its Pharmacodynamic and Pharmacokinetic Properties, and Therapeutic Efficacy, in Ischaemic Heart Disease, Hypertension and Related Cardiovascular Disorders
2. 2,3,8,8a-Tetrahydro-7H-oxazolo[3,2-a]pyridine: A new heterocyclic system
3. Regiochemistry in the synthesis of 2,3,8,8a-tetrahydro-7H-oxazolo[3,2-a]pyridines
4. Synthesis of Enantiopure 2,3,8,8a- Tetrahydro-7H-oxazolo[3,2-a]pyridine Derivatives
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1. Chemistry of bicyclic 5-6 systems: Synthesis of oxazolo[3,2-a]pyridines and their salts with a ring-junction nitrogen atom;Synthetic Communications;2019-07-23
2. Domino-Ring Opening-Cyclization (DROC) of Donor-Acceptor (DA) Cyclopropanes;Israel Journal of Chemistry;2016-02-16
3. A facile and highly convergent approach to thiazolo[3,2-a]pyridines via one-pot multicomponent domino reaction under metal-free and solvent-free conditions;Tetrahedron;2015-05
4. A Route to Highly Functionalized β-Enaminoesters via a Domino Ring-Opening Cyclization/Decarboxylative Tautomerization Sequence of Donor–Acceptor Cyclopropanes with Substituted Malononitriles;Organic Letters;2014-04-08
5. Oxazolo[3,2-a]pyridine. A new structural scaffold for the reversal of multi-drug resistance in Leishmania;Bioorganic & Medicinal Chemistry Letters;2012-10
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