Advances in the Baylis–Hillman reaction-assisted synthesis of cyclic frameworks
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference323 articles.
1. Target-Oriented and Diversity-Oriented Organic Synthesis in Drug Discovery
2. Generating Diverse Skeletons of Small Molecules Combinatorially
3. The Baylis–Hillman reaction: a novel source of attraction, opportunities, and challenges in synthetic chemistry
4. Morita, K. Japan Patent 6803364, 1968;
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1. A Formal [3+3] Annulation of Morita–Baylis–Hillman Ketones to Construct Pyrimidobenzothiazoles;Synthesis;2024-07-25
2. Morita–Baylis–Hillman Spirannulation under Phosphine- and Anion-Binding Catalysis;Organic Letters;2024-04-08
3. A retro-Mannich mediated transformation of Morita–Baylis–Hillman ketones to saturated imidazo[1,2-a]pyridines;Organic Chemistry Frontiers;2024
4. A facile synthesis of (E)-5-arylylidene-3-((substituted-ind-2-en-1-one)methyl)-3-aryl piperidine-2,6-diones via domino bis-cyclization using the Baylis-Hillman adducts;Tetrahedron;2023-09
5. Baylis–Hillmanadducts as an important synthon for the synthesis of α‐carbolinone and α‐carboline derivatives;Journal of Heterocyclic Chemistry;2023-03-06
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