Synthesis of poly-substituted benzenes starting from Baylis–Hillman adducts: DBU-assisted unusual dehydrogenation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference41 articles.
1. For the synthesis of various aromatic and hetero-aromatic compounds from the Baylis–Hillman adducts, see:
2. Trifluoroacetic acid: a more effective and efficient reagent for the synthesis of 3-arylmethylene-3,4-dihydro-1H-quinolin-2-ones and 3-arylmethyl-2-amino-quinolines from Baylis–Hillman derivatives via Claisen rearrangement
3. Synthesis of Substituted 1H- and 3H-1-Benzazepines and Rearrangement of Alkyl 1H-1-Benzazepine-2-carboxylates into Isoquinolines
4. The Baylis–Hillman approach to quinoline derivatives
5. Synthesis of poly-substituted nitrobenzene derivatives from Baylis–Hillman adducts via [3+3] annulation protocol
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2. Umpolung cyclization reaction of N-cinnamoylthioureas in the presence of DBU;Organic & Biomolecular Chemistry;2018
3. Synthesis of Poly-Substituted Benzene from Morita-Baylis-Hillman Adducts Via [3 + 1 + 2] Annulation Strategy: Palladium-catalyzed Domino Cyclization (5-exo/3-exo), Ring-Expansion by Palladium Rearrangement, and Aromatization;Bulletin of the Korean Chemical Society;2016-01-14
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