Baylis-Hillman Reaction
Theoretical study on DABCO-catalyzed ring expansion of cyclopropyl ketone: Mechanism, chemoselectivity, and role of catalyst - ScienceDirect
DABCO - Wikipedia
1,4-Diazabicyclo 2.2.2 octane ReagentPlus , = 99 280-57-9
DABCO‐Catalysed Amidation under Assistance of Aerial Oxidation: Access to α‐ketoamides - Monga - 2018 - ChemistrySelect - Wiley Online Library
DABCO - Wikipedia
New dicationic DABCO-based ionic liquids: a scalable metal-free one-pot synthesis of bis-2-amino-5-arylidenethiazol-4-ones | Royal Society Open Science
Nucleophilic Organic Base DABCO-Mediated Chemospecific Meinwald Rearrangement of Terminal Epoxides into Methyl Ketones | The Journal of Organic Chemistry
DABCO - American Chemical Society
The structure of Tröger's base (stereochemistry not shown) and DABCO | Download Scientific Diagram
DABCO as a Base and an Organocatalyst in Organic Synthesis: A Review | Bentham Science
![1,4-Diazabicyclo[2.2.2]octane (DABCO) as a useful catalyst in organic synthesis | Bita | European Journal of Chemistry](http://www.eurjchem.com/public/site/images/arslanh/1_1_54_60_800.png "1,4-Diazabicyclo[2.2.2]octane (DABCO) as a useful catalyst in organic synthesis | Bita | European Journal of Chemistry")
1,4-Diazabicyclo[2.2.2]octane (DABCO) as a useful catalyst in organic synthesis | Bita | European Journal of Chemistry
DABCO bond cleavage for the synthesis of piperazine derivatives - RSC Advances (RSC Publishing) DOI:10.1039/C9RA07870C
The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 1. Catalysis of Morita–Baylis–Hillman and Knoevenagel reactions | SpringerLink
DABCO as a practical catalyst for aromatic halogenation with N-halosuccinimides - RSC Advances (RSC Publishing)
Lewis Base‐Brønsted Acid Co‐catalyzed Morita‐Baylis‐Hillman Reaction of Cyclic Sulfamidate Imines - Khassenova - 2021 - European Journal of Organic Chemistry - Wiley Online Library
The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 1. Catalysis of Morita–Baylis–Hillman and Knoevenagel reactions | SpringerLink
DABCO as a green catalyst for the synthesis of pyranoquinoline derivatives
Structures of the Dabco‐base ionic liquid catalysts | Download Scientific Diagram
Baylis-Hillman Reaction - an overview | ScienceDirect Topics
SOLVED: 2) The reaction sequence below results in product 2.1 The first step is a Baylis-Hillman reaction. Note that DABCO is only involved in the first step of the reaction sequence and
DABCO - Wikipedia
Nucleophilic Organic Base DABCO-Mediated Chemospecific Meinwald Rearrangement of Terminal Epoxides into Methyl Ketones | The Journal of Organic Chemistry
Nucleophilic Organic Base DABCO-Mediated Chemospecific Meinwald Rearrangement of Terminal Epoxides into Methyl Ketones | The Journal of Organic Chemistry
Dual Nucleophilic Catalysis with DABCO for the N-Methylation of Indoles | The Journal of Organic Chemistry
The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 1. Catalysis of Morita–Baylis–Hillman and Knoevenagel reactions | SpringerLink
