Study of the Baylis−Hillman Reaction in a Microreactor Environment: First Continuous Production of Baylis−Hillman Adducts
Author:
Affiliation:
1. Research Group SynBioC, Department of Organic Chemistry, Faculty of Bioscience Engineering, Ghent University, Coupure links 653, B-9000 Ghent, Belgium
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/op050228c
Reference71 articles.
1. Applications of Baylis–Hillman acetates: one-pot, facile and convenient synthesis of substituted γ-lactams
2. Straightforward Asymmetric Entry to Highly Functionalized 3-Substituted 3-Hydroxy-β-lactams via Baylis−Hillman or Bromoallylation Reactions
3. DYKAT of Baylis−Hillman Adducts: Concise Total Synthesis of Furaquinocin E
4. Baylis–Hillman reaction assisted parallel synthesis of 3,5-disubstituted isoxazoles and their in vivo bioevaluation as antithrombotic agents
5. Baylis-Hillman Reaction Assisted Synthesis of Substituted 5,8-Dihydroisoxazolo[4,5-c]azepin-4-ones: A Novel Isoxazole-Annulated Heterocycle
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