Transition Metal‐Catalyzed Transformations of Chalcones
CMM Santos, AMS Silva - The Chemical Record, 2024 - Wiley Online Library
Chalcones are a class of naturally occurring flavonoid compounds associated to a variety of
biological and pharmacological properties. Several reviews have been published describing …
biological and pharmacological properties. Several reviews have been published describing …
Chalcones and bis-chalcones: As potential α-amylase inhibitors; synthesis, in vitro screening, and molecular modelling studies
Despite of a diverse range of biological activities associated with chalcones and bis-
chalcones, they are still neglected by the medicinal chemist for their possible α-amylase …
chalcones, they are still neglected by the medicinal chemist for their possible α-amylase …
Synthesis of fluorinated alkyl aryl ethers by palladium-catalyzed C–O cross-coupling
R Szpera, PG Isenegger, M Ghosez… - Organic …, 2020 - ACS Publications
Herein, we report a highly effective protocol for the cross-coupling of (hetero) aryl bromides
with fluorinated alcohols using the commercially available precatalyst tBuBrettPhos Pd G3 …
with fluorinated alcohols using the commercially available precatalyst tBuBrettPhos Pd G3 …
Orchestrating a β-hydride elimination pathway in palladium (II)-catalyzed arylation/alkenylation of cyclopropanols using organoboron reagents
T Ramar, MAM Subbaiah… - The Journal of Organic …, 2022 - ACS Publications
The scope of chemoselective β-hydride elimination in the context of arylation/alkenylation of
homoenolates from cyclopropanol precursors using organoboronic reagents as …
homoenolates from cyclopropanol precursors using organoboronic reagents as …
An Easy Access to Oxime Ethers by Pd‐Catalyzed C—O Cross‐Coupling of Activated Aryl Bromides with Ketoximes and Chalcone Oximes
Summary of main observation and conclusion An efficient Pd‐catalyzed method for C—O
cross‐coupling of ketoximes and chalcone oximes with activated aryl bromides and bromo …
cross‐coupling of ketoximes and chalcone oximes with activated aryl bromides and bromo …
Total Synthesis and Anti-Inflammatory Activity of Velutone F
Y Li, M Wu, H Dong, P Yu, L Lu… - Natural Product …, 2022 - journals.sagepub.com
Velutone F (1), a natural bioactive chalcone isolated from Millettia velutina Dunn, possesses
significant anti-inflammatory activity. In this study, we have accomplished the total synthesis …
significant anti-inflammatory activity. In this study, we have accomplished the total synthesis …
Synthesis and Evaluation of Antiplasmodial Activity of 2,2,2-Trifluoroethoxychalcones and 2-Fluoroethoxy Chalcones against Plasmodium falciparum in Culture
A new class of compounds comprising two series of chalcones with 2, 2, 2-trifluoroethoxy
group and 2-fluoroethoxy groups were synthesized and screened for in vitro antiplasmodial …
group and 2-fluoroethoxy groups were synthesized and screened for in vitro antiplasmodial …
Synthesis of novel chalcones through palladium-catalyzed CO cross-coupling reaction of bromo-chalcones with ethyl acetohydroxamate and their antiplasmodial …
R Vinoth, TM Rangarajan, RP Singh, M Singh - Bioorganic Chemistry, 2019 - Elsevier
An efficient method for palladium-catalyzed Csingle bond O cross-coupling of ethyl
acetohydroxamate (EAcHO) with 4-bromo-chalcones has been developed to synthesize …
acetohydroxamate (EAcHO) with 4-bromo-chalcones has been developed to synthesize …
Chemical Transformations of Methanol
Z Chen, XF Wu - The Chemical Transformations of C1 …, 2022 - Wiley Online Library
The applications of methanol in organic chemistry have been summarized and discussed
here. Methanol has been used in various transformations including methylation …
here. Methanol has been used in various transformations including methylation …
Bis (1, 1‐dimethylethyl)[2′, 4′, 6′‐tris‐(1‐methylethyl)[1, 1′‐biphenyl]‐2‐yl]‐phosphine and Dicyclohexyl [2′, 4′, 6′‐tris (1‐methylethyl)[1, 1′‐biphenyl]‐2‐yl] …
E Herrero‐Gómez… - Encyclopedia of Reagents …, 2001 - Wiley Online Library
Abstract InChI= 1S/C33H49P/c1‐23 (2) 26‐21‐30 (24 (3) 4) 33 (31 (22‐26) 25 (5) 6) 29‐19‐
13‐14‐20‐32 (29) 34 (27‐15‐9‐7‐10‐16‐27) 28‐17‐11‐8‐12‐18‐28/h13‐14, 19‐25, 27 …
13‐14‐20‐32 (29) 34 (27‐15‐9‐7‐10‐16‐27) 28‐17‐11‐8‐12‐18‐28/h13‐14, 19‐25, 27 …