Diastereoselective Synthesis of Spiro[pyrazolone-4,3′-tetrahydrothiophenes] via a Sulfa-Michael/Aldol Domino Reaction
Author:
Affiliation:
1. Institute of Organic Chemistry, RWTH Aachen University
2. Department of Chemistry, Nanoscience Center, University of Jyvaskyla
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry,Catalysis
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0035-1562473.pdf
Cited by 15 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Diversity-Oriented Synthesis of Spiro[chromeno[2,3-b]pyridine-3,4′-pyrazole] Derivatives via Pseudo-Three-Component Reactions;The Journal of Organic Chemistry;2024-07-09
2. Synthesis and Biological Evaluation of Some Sulfur-Containing Spiro Compounds;S-Heterocycles;2024
3. One-pot synthesis of 2-thioxothiazolidin-4-one, thiazolidine-2,4-dione, 2-iminothiazolidin-4-one based spiro-thiolane and bicyclic chromene-thiolane hybrids via Knoevenagel, 1,4-sulfa-Michael and aldol reactions;Arkivoc;2023-05-05
4. Asymmetric Synthesis of Spiropyrazolone-Fused Dihydrofuran-naphthoquinones Bearing Contiguous Stereocenters via a Michael Addition/Chlorination/Nucleophilic Substitution Sequence;The Journal of Organic Chemistry;2023-03-22
5. Recent Advances in Base-assisted Michael Addition Reactions;Current Organic Chemistry;2022-07
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