Stereoselective C−B and C−H Bonds Functionalization of polyBorylated Alkenes [PDF]
Alkenes are fundamental functional groups which feature in various materials and bioactive molecules; however, efficient divergent strategies for their stereodefined synthesis are difficult.
Narendra K., Vaishanv +3 more
core +1 more source
Transition-metal-free electrochemical-induced active C(sp3)-H functionalization
Direct C–H bond functionalization is the most effective technique to construct C–X (X = C, N, O, S, etc.), which could simplify the conventional synthesis methods.
Xiaolong Ma +4 more
doaj +1 more source
Radical‐Promoted Distal C‐H Functionalization of C(sp3) Centers with Fluorinated Moieties
International audienceDue to their unique properties, fluorinated scaffolds are pivotal compounds in pharmaceuticals, agrochemicals and materials science.
Tatiana Besset +5 more
core +1 more source
Multitask Prediction of Site Selectivity in Aromatic C-H Functionalization Reactions [PDF]
Aromatic C-H functionalization reactions are an important part of the synthetic chemistry toolbox. Accurate prediction of site selectivity can be crucial for prioritizing target compounds and synthetic routes in both drug discovery and process chemistry.
Klavs F. Jensen (5815258) +8 more
core +1 more source
Enantioselective Single and Dual a-C–H Bond Functionalization of Cyclic Amines via Enzymatic Carbene Transfer [PDF]
Cyclic amines are ubiquitous structural motifs found in pharmaceuticals and biologically active natural products, making methods for their elaboration via direct C–H functionalization of considerable synthetic value.
Bo M. , Couture +5 more
core +2 more sources
Strategies to transform remote C(sp3)-H bonds of amino acid derivatives
Amino acids and peptides play an important role in nature as well as in the pharmaceutical industry. Therefore, transformation of amino acids and peptides into their unnatural derivatives via step and atom economical ways is highly demanding. Although, a
Supreeta Sen +2 more
doaj +1 more source
Organocatalytic Asymmetric α-C-H Functionalization of Alkyl Amines [PDF]
Catalytic enantioselective α-C–H functionalization of achiral amines could provide an ideal synthetic approach toward chiral amines. The alkyl amines constitute the most diverse and synthetically important class of achiral amines.
Cheng, Cheng +9 more
core +2 more sources
C-H Functionalization Reactions of Unprotected N-Heterocycles by Gold Catalyzed Carbene Transfer [PDF]
The C-H functionalization reaction of N-heterocycles with unprotected N-H group is one of the most step-economic strategies to introduce functional groups without the need of installation and removal of protecting groups.
Polina, Aseeva +5 more
core +2 more sources
Use of Emerging C–H Functionalization Methods to Implement Strategies for the Divergent Total Syntheses of Bridged Polycyclic Natural Products [PDF]
Carbon–hydrogen (C–H) bonds are ubiquitous in complex natural products. Over the past three decades, many methods to convert C–H bonds distal from functional groups, which were generally considered inert, have been developed.
Richmond, Sarpong, Goh, Sennari
core +1 more source
C-H Functionalization via Iron-Catalyzed Carbene-Transfer Reactions
The direct C-H functionalization reaction is one of the most efficient strategies by which to introduce new functional groups into small organic molecules.
Claire Empel +2 more
doaj +1 more source

