Articles with "sterically demanding" as a keyword



Highly Active Catalyst for Suzuki-Miyaura Coupling to Form Sterically Demanding Biaryls: Electronic Control of Pd through the Secondary Interaction Using a Buchwald-Type Ligand Bearing a Fluorinated Aryl Ring.

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Published in 2025 at "Organic letters"

DOI: 10.1021/acs.orglett.5c01467

Abstract: To accelerate reductive elimination in Suzuki-Miyaura coupling (SMC) through secondary interactions with a Buchwald-type ligand, a heptafluorotolyl group was introduced into the ligand's structure, guided by DFT calculations. The resulting ligand, HFTPhos, was effective for… read more here.

Keywords: type ligand; suzuki miyaura; ligand; buchwald type ... See more keywords

Rational Engineered C-Acyltransferase Transforms Sterically Demanding Acyl Donors

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Published in 2020 at "ACS Catalysis"

DOI: 10.1021/acscatal.9b04617

Abstract: The biocatalytic Friedel–Crafts acylation has been identified recently for the acetylation of resorcinol using activated acetic acid esters for the synthesis of acetophenone derivatives catalyzed by an acyltransferase. Because the wild-type enzyme is limited to… read more here.

Keywords: engineered acyltransferase; transforms sterically; rational engineered; acyltransferase transforms ... See more keywords

Formation of silaimines from a sterically demanding iminophosphonamido chlorosilylene via intramolecular N-P bond cleavage.

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Published in 2021 at "Chemical communications"

DOI: 10.1039/d1cc02812j

Abstract: The sterically demanding iminophosphonamido chlorosilylene [Ph2P(DipN)2]SiCl (Dip = 2,6-diisopropylphenyl) was synthesized and fully characterized using NMR spectroscopy and X-ray crystallography. Substitution reactions of [Ph2P(DipN)2]SiCl with N- and Fe-nucleophiles led to the unexpected formation of the… read more here.

Keywords: intramolecular bond; sterically demanding; via intramolecular; demanding iminophosphonamido ... See more keywords

A synthetic tactic to substitute axial ligands in sterically demanding Ru(II)porphyrinates.

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Published in 2022 at "Dalton transactions"

DOI: 10.1039/d2dt01095j

Abstract: We report a synthetic strategy that allows for the preparation of sterically encumbered heteroleptic Ru(II)porphyrinates with the desired configuration of stable/inert and weak/labile axial ligands to direct reactions between substrates to exclusively occur at the… read more here.

Keywords: tactic substitute; substitute axial; axial ligands; sterically demanding ... See more keywords

C–C Coupling in sterically demanding porphyrin environments

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Published in 2024 at "Beilstein Journal of Organic Chemistry"

DOI: 10.3762/bjoc.20.234

Abstract: Unlike their planar counterparts, classic synthetic protocols for C–C bond forming reactions on nonplanar porphyrins are underdeveloped. The development of C–C bond forming reactions on nonplanar porphyrins is critical in advancing this field of study… read more here.

Keywords: chemistry; porphyrin; coupling sterically; demanding porphyrin ... See more keywords