Articles with "binol" as a keyword



Synthesis of a newly modified poly-H 8 -BINOL ligand and its applications in the asymmetric addition of triethylaluminium to aromatic aldehydes

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Published in 2017 at "Chemical Research in Chinese Universities"

DOI: 10.1007/s40242-017-7093-y

Abstract: A new H8-BINOL polymer was synthesized by radical polymerization and proved to be an effective catalyst in enantioselective addition of triethylaluminium to aromatic aldehydes in the presence of titanium isopropoxide. The polymer can be prepared… read more here.

Keywords: binol; triethylaluminium aromatic; aromatic aldehydes; addition triethylaluminium ... See more keywords

Intramolecular chirality induction and intermolecular chirality modulation in BINOL bridged bisporphyrin hosts

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Published in 2017 at "Dyes and Pigments"

DOI: 10.1016/j.dyepig.2016.11.006

Abstract: Abstract We have studied the intra- and inter-molecular chirogenesis events on a family of chiral bisporphyrin hosts H1-H3 . The three pairs of enantiomers for H1-H3 were constructed by connecting two zinc(II) porphyrinates to a… read more here.

Keywords: chirality induction; chirality; bisporphyrin hosts; binol ... See more keywords

Regioselective Substitution of BINOL

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Published in 2024 at "Chemical Reviews"

DOI: 10.1021/acs.chemrev.4c00132

Abstract: 1,1′-Bi-2-naphthol (BINOL) has been extensively used as the chirality source in the fields of molecular recognition, asymmetric synthesis, and materials science. The direct electrophilic substitution at the aromatic rings of the optically active BINOL has… read more here.

Keywords: substitution; binol; regioselective substitution; substitution binol ... See more keywords

Dynamic Thermodynamic Resolution of Racemic 1,1'-Binaphthyl-2,2'-diol (BINOL).

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Published in 2024 at "Organic letters"

DOI: 10.1021/acs.orglett.4c00520

Abstract: A dynamic thermodynamic resolution method for converting (R/S)-BINOL (1,1'-binaphthyl-2,2'-diol) into (R)-BINOL in 100% theoretical yield is reported. This technique involves mixing (R/S)-BINOL with N-benzyl cinchonidinium bromide (1 equiv) and a [Cu2(tmeda)2(μ-OH)2]Br2 (2.5 mol %) redox… read more here.

Keywords: thermodynamic resolution; diol binol; binaphthyl diol; dynamic thermodynamic ... See more keywords

Crown Ether-Derived Chiral BINOL: Enantioselective Michael Addition of Alkenyl Boronic Acids to α,β-Unsaturated Ketones

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Published in 2021 at "ACS Omega"

DOI: 10.1021/acsomega.1c05875

Abstract: A new class of aza-crown ether-derived chiral BINOL catalysts were designed, synthesized, and applied in the asymmetric Michael addition of alkenylboronic acids to α,β-unsaturated ketones. It was found that introducing aza-crown ethers to the BINOL… read more here.

Keywords: derived chiral; ether derived; chiral binol; crown ether ... See more keywords

Synthesis and stereochemistry of helical polyurethanes based on 2,2′-dihydroxy-1,1′-binaphthyl and diisocyanatobenzenes

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Published in 2020 at "Polymer Chemistry"

DOI: 10.1039/c9py01348b

Abstract: Polyaddition between 2,2′-dihydroxy-1,1′-binaphthyl (BINOL) and 1,4-diisocyanatobenzene (14DIB) and that between BINOL and 1,3-diisocyanatobenzene (13DIB) were conducted leading to optically active, helical polyurethanes, poly(BINOL-alt-14DIB) and poly(BINOL-alt-13DIB), respectively. In BINOL-14DIB systems, cyclic dimers were formed along with… read more here.

Keywords: dihydroxy binaphthyl; binol units; poly binol; binol alt ... See more keywords

Chiral BINOL-based borate counterions: from cautionary tale on anion stability to enantioselective Cu-catalyzed cyclopropanation.

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Published in 2022 at "Chemical communications"

DOI: 10.1039/d2cc05924j

Abstract: The chiral weakly coordinating (3,3'-biphenyl-BINOL)BF2 anion can be generated by the reaction of the BINOL derivative with Cu(NCMe)4BF4. Structural analysis suggest the anion is weakly coordinating to Cu+. However, its use in cyclopropanation reactions leads… read more here.

Keywords: based borate; binol; cyclopropanation; binol based ... See more keywords

Spirobifluorene-BINOL-based microporous polymer nanoreactor for efficient 1H-tetrazole synthesis and iodine adsorption with facile charge transfer.

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Published in 2024 at "Nanoscale"

DOI: 10.1039/d4nr00599f

Abstract: Porous polymeric nanoreactors capable of multitasking are attractive and require a judicious design strategy. Herein, we describe an unusual approach for the synthesis of a porous polymer SBF-BINOL-6 by in situ formation of the BINOL… read more here.

Keywords: charge transfer; synthesis; polymer; iodine adsorption ... See more keywords

Changing the absolute configuration of atropisomeric bisnaphthols (BINOLs).

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Published in 2025 at "Chemical communications"

DOI: 10.1039/d5cc01026h

Abstract: Bisnaphthol (BINOL) is a ubiquitous core skeleton in versatile chiral catalysts and ligands for transition metals, and this representative atropisomeric structure also serves as a building block in various optically active natural products. Due to… read more here.

Keywords: changing absolute; kinetic resolution; binol; absolute configuration ... See more keywords

Luminescent Behavior of Zn(II) and Mn(II) Halide Derivatives of 4-Phenyldinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepine 4-Oxide and Single-Crystal X-ray Structure Determination of the Ligand

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Published in 2024 at "Molecules"

DOI: 10.3390/molecules29010239

Abstract: The two enantiomers of chiral phosphonate 4-phenyldinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepine 4-oxide, O=PPh(BINOL), were synthesized from the proper 1,1′-bi-2-naphtol (BINOL) enantiomer and characterized. The structure of the (S)-enantiomer was elucidated by means of single-crystal X-ray diffraction. The reaction with… read more here.

Keywords: structure; phenyldinaphtho dioxaphosphepine; crystal ray; single crystal ... See more keywords