Recent advances in the Baylis− Hillman reaction and applications

D Basavaiah, AJ Rao, T Satyanarayana - Chemical reviews, 2003 - ACS Publications
The carbon-carbon bond formation and the functional group transformations are the most
fundamental reactions for the construction of a molecular framework and hence represent a …

Innovative extraction technologies of bioactive compounds from plant by-products for textile colorants and antimicrobial agents

TL Nguyen, A Ora, ST Häkkinen, A Ritala… - Biomass conversion and …, 2024 - Springer
The agriculture and horticulture industries generate many by-products while processing
commodities, leading to significant environmental and societal dilemmas. Bioactive …

Asymmetric domino reactions. Part A: Reactions based on the use of chiral auxiliaries

H Pellissier - Tetrahedron, 2006 - Elsevier
Conclusions The first part of this review clearly demonstrates the diversity and power of
asymmetric domino reactions based on the use of chiral auxiliaries in the field of synthetic …

Mechanism of the Morita− Baylis− Hillman reaction: A computational investigation

R Robiette, VK Aggarwal… - Journal of the American …, 2007 - ACS Publications
Accurate calculations are presented on the mechanism of the MBH reaction, focusing on the
reaction between methyl acrylate and benzaldehyde, catalyzed by a tertiary amine. We …

Baylis− Hillman mechanism: A new Interpretation in aprotic solvents

KE Price, SJ Broadwater, HM Jung… - Organic Letters, 2005 - ACS Publications
Using reaction rate data collected in aprotic solvents, we have determined that the Baylis−
Hillman rate-determining step is second order in aldehyde and first order in DABCO and …

Dramatic Rate Acceleration of the Baylis− Hillman Reaction in Homogeneous Medium in the Presence of Water

J Cai, Z Zhou, G Zhao, C Tang - Organic Letters, 2002 - ACS Publications
In homogeneous H2O/solvent medium, the reaction rate of aromatic aldehydes and
acrylonitrile or acrylate was greatly accelerated, which led to shorter reaction time, lower …

Ab Initio and density functional theory evidence on the rate-limiting step in the Morita− Baylis− Hillman reaction

D Roy, RB Sunoj - Organic letters, 2007 - ACS Publications
The first ab initio and DFT studies on the mechanism of the MBH reaction show that the rate-
limiting step involves an intramolecular proton transfer in the zwitterionic intermediate …

Diastereoselective Baylis− Hillman Reactions: The Design and Synthesis of a Novel Camphor-Based Chiral Auxiliary

KS Yang, K Chen - Organic letters, 2000 - ACS Publications
Reaction of chiral acryloylhydrazide 5 derived from novel auxiliary 4 with aldehydes in the
presence of DABCO affords practical levels (up to 98% de) of β-hydroxy-α-methylene …

Acylvinyl and vinylogous synthons

R Chinchilla, C Nájera - Chemical Reviews, 2000 - ACS Publications
The functionality-(CHdCH) nCO-is an important structural feature in many naturally occurring
compounds such as oxopolyenoic acids, lactones, and polyenamides. 1 Consequently …

Morita–Baylis–Hillman reactions between conjugated nitroalkenes or nitrodienes and carbonyl compounds

I Deb, P Shanbhag, SM Mobin, INN Namboothiri - 2009 - Wiley Online Library
Abstract Morita–Baylis–Hillman (MBH) reactions between conjugated nitroalkenes or
nitrodienes and various carbonyl compounds such as glyoxylate, trifluoropyruvate …