Synthesis of indolizines from pyridinium 1,4-zwitterionic thiolates and propiolic acid derivatives via a formal [4 + 1] pathway
Author:
Affiliation:
1. State Key Laboratory of Applied Organic Chemistry
2. College of Chemistry and Chemical Engineering
3. Lanzhou University
4. Lanzhou 730000
5. China
6. Institute of Marine Biomedicine
7. Shenzhen Polytechnic
8. Shenzhen 518055
Abstract
Indolizines were synthesized from 1,4-zwitterionic thiolates and propiolic acid derivatives mediated by triethylamine via a formal [4 + 1] pathway.
Funder
National Natural Science Foundation of China
Ministry of Education of the People's Republic of China
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/OB/D0OB01398F
Reference43 articles.
1. Pyridinium 1,4-zwitterionic thiolates as a useful class of sulfur-containing synthons: application to the synthesis of 2,5-dihydro-1,4,5-thiadiazepines
2. Synthesis of tetrasubstituted thiophenes via a [3+2] cascade cyclization reaction of pyridinium 1,4-zwitterionic thiolates and activated allenes
3. Development and Application of Pyridinium 1,4-Zwitterionic Thiolates: Synthesis of Polysubstituted Thiophenes
4. Synthesis of fully substituted pyrazoles from pyridinium 1,4-zwitterionic thiolates and hydrazonoyl chlorides via a [[3 + 3] − 1] pathway
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5. Copper-Catalyzed Formal [4 + 1] Annulation toward Diverse Trifunctionalized Indolizines from Pyridinium 1,4-Zwitterionic Thiolates and Diazos;The Journal of Organic Chemistry;2023-05-12
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