Intramolecular Morita–Baylis–Hillman and Rauhut–Currier reactions. A catalytic and atom economic route for carbocycles and heterocycles
KC Bharadwaj - RSC advances, 2015 - pubs.rsc.org
Intramolecular Morita–Baylis–Hillman and Rauhut–Currier reactions are important tools
which have constantly grown over several years. This review summarizes and highlights …
which have constantly grown over several years. This review summarizes and highlights …
The versatility of DABCO: synthetic applications of its basic, nucleophilic, and catalytic properties Part 1. Catalysis of Morita–Baylis–Hillman and Knoevenagel …
DI Bugaenko, AV Karchava, MA Yurovskaya - Chemistry of Heterocyclic …, 2020 - Springer
This review article covers literature data from the last 5 years regarding the various
applications of 1, 4-diazabicyclo [2.2. 2] octane (DABCO) in organic chemistry. The frequent …
applications of 1, 4-diazabicyclo [2.2. 2] octane (DABCO) in organic chemistry. The frequent …
Applications of the Morita–Baylis–Hillman reaction in the synthesis of heterocyclic systems
PT Kaye - Advances in Heterocyclic Chemistry, 2019 - Elsevier
Abstract The Morita–Baylis–Hillman (MBH) reaction has been the subject of a number of
significant earlier reviews and continues to enjoy widespread application as an intrinsically …
significant earlier reviews and continues to enjoy widespread application as an intrinsically …
Chemoselective Intramolecular Morita–Baylis–Hillman Reaction; Acrylamide and Ketone as Sluggish Reacting Partners on a Labile Framework
KC Bharadwaj - The Journal of Organic Chemistry, 2024 - ACS Publications
Chemoselectivity is an important issue frequently encountered while working over labile
precursors. Carbonyl compounds with a heteroatom at the β carbon are sensitive precursors …
precursors. Carbonyl compounds with a heteroatom at the β carbon are sensitive precursors …
N-Benzyloxyacrylamides as Bisnucleophiles in an Organocatalyzed Domino aza-Michael/Morita-Baylis-Hillman Sequence
I Alahyen, C Taillier, J Lhoste, V Dalla… - Organic Letters, 2024 - ACS Publications
We herein describe a stereoselective organocatalyzed aza-Michael/Morita-Baylis-Hillman
domino reaction between readily accessible acrylamides and α, β-unsaturated carbonyls …
domino reaction between readily accessible acrylamides and α, β-unsaturated carbonyls …
Chemoselective and Highly Rate Accelerated Intramolecular Aza-Morita–Baylis–Hillman Reaction
KC Bharadwaj - The Journal of Organic Chemistry, 2018 - ACS Publications
Despite being a very useful C–C bond forming and highly applicative reaction, Morita–Baylis–
Hillman (MBH) reaction has been limited by its excessive slow reaction rate, including its …
Hillman (MBH) reaction has been limited by its excessive slow reaction rate, including its …
Chemoselective Intramolecular Rauhut‐Currier Reaction on a Labile Framework of Enone and Acrylamide: Tricyclohexylphosphine as a Stable and Economical …
RK Verma, M Bairwa… - European Journal of …, 2024 - Wiley Online Library
Abstract Intramolecular Rauhut‐Currier (IRC) reaction is an atom‐economical way of making
carbocyclic and heterocyclic rings. However, its sensitivity towards electronic and steric …
carbocyclic and heterocyclic rings. However, its sensitivity towards electronic and steric …
Acryl activation by intramolecular hydrogen bond: Morita Baylis Hillman reaction of acrylamide with broad substrate scope
KC Bharadwaj - ChemistrySelect, 2017 - Wiley Online Library
Use of acrylamide as an activated alkene in largely recognized Morita Baylis Hillman (MBH)
reaction has been least explored owing to less reactivity of acrylamide as Michael acceptor …
reaction has been least explored owing to less reactivity of acrylamide as Michael acceptor …
[PDF][PDF] Intramolecular Baylis-Hillman reaction: synthesis of heterocyclic molecules
D Basavaiah, GC Reddy - Arkivoc, 2016 - pdfs.semanticscholar.org
Abstract The Baylis-Hillman (BH)[also known as the Morita-Baylis-Hillman (MBH)] reaction is
a versatile atom-economic CC bond forming reaction between the α-position of activated …
a versatile atom-economic CC bond forming reaction between the α-position of activated …
Theoretical investigation into the coordination of R‐/S‐asymmetric uranyl–salophens containing six‐membered ring lactam with cis−/trans‐cyclohexylamines
LL Yang, XH Kong, ZL Wu, YW Lin… - Applied …, 2018 - Wiley Online Library
A six‐membered ring lactam derivative was introduced in a parallel manner into uranyl–
salophens with R/S configuration (R‐/S‐AUSRLs), which were used as receptors to …
salophens with R/S configuration (R‐/S‐AUSRLs), which were used as receptors to …