Highly Stereoselective Synthesis of 2-Acyl-3-sulfonamidobut-2-enoates Using Solid Calcium Carbide as a Substitute for Gaseous Acetylene
Author:
Affiliation:
1. College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou, Gansu 730070, P. R. China
Funder
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c02275
Reference34 articles.
1. One-Pot Synthesis of Highly Substituted Nicotinic Acid Derivatives Based on a Formylation Strategy of Enamino Keto Esters
2. Four-Component Synthesis of Functionalized 2,2′-Bipyridines Based on the Blaise Reaction
3. One pot synthesis of unsaturated enaminoketoesters or of pyridines in the tin(IV) chloride-promoted reactions of β-ketoesters with α,β-unsaturated nitriles
4. Reactions of enamino keto esters of 1,2,3,4-tetrahydroisoquinoline series with nucleophiles
5. Chemoselective Synthesis of Pyrazole Derivatives via b-Enamino Keto Esters
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