Articles with "catalyzed highly" as a keyword



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Copper-Catalyzed Highly Selective Hydrosilylation of Silyl or Boryl Alkene: A Method for Preparing Chiral Geminated Disilyl and Borylsilyl Reagents.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c00858

Abstract: The copper-catalyzed highly selective hydrosilylation of silyl or boryl alkene has been developed. This chemistry could afford a practical method for preparing chiral geminated disilyl and borylsilyl reagents, which are useful organosilanes and versatile synthons… read more here.

Keywords: chemistry; selective hydrosilylation; hydrosilylation silyl; copper catalyzed ... See more keywords

Rhodium-Catalyzed Highly Enantio- and Diastereoselective Alkenylation of β,γ-Unsaturated Butenolides via Dynamic Kinetic Resolution.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c03551

Abstract: A rhodium-catalyzed highly enantio- and diastereoselective alkenylation of β,γ-unsaturated butenolides is reported. The use of a chiral diene ligand, (S,S)-Ph-bod, enables the facile synthesis of chiral butyrolactones in high yields with extremely high enantioselectivities (>99%… read more here.

Keywords: alkenylation; enantio diastereoselective; rhodium catalyzed; unsaturated butenolides ... See more keywords
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Chiral Imidodiphosphoric Acid-Catalyzed Highly Diastereo- and Enantioselective Synthesis of Poly-Substituted 3,4-Dihydro-2 H-pyrans: [4 + 2] Cycloadditions of β,γ-Unsaturated α-Ketoesters and 3-Vinylindoles.

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Published in 2019 at "Organic letters"

DOI: 10.1021/acs.orglett.9b01675

Abstract: Imidodiphosphoric acids were employed to catalyze inverse-electron-demand hetero-Diels-Alder reaction of β,γ-unsaturated α-ketoesters and 3-vinylindoles. A series of optically active 3,4-dihydro-2 H-pyran derivatives with three contiguous stereogenic centers was synthesized in excellent yields (70-99%), diastereoselectivities (>20:1),… read more here.

Keywords: ketoesters vinylindoles; imidodiphosphoric acid; catalyzed highly; chiral imidodiphosphoric ... See more keywords
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Gold(I)-Catalyzed Highly Enantioselective [4 + 2]-Annulations of Cyclopentadienes with Nitrosoarenes via Nitroso-Povarov versus Oxidative Nitroso-Povarov Reactions

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Published in 2020 at "ACS Catalysis"

DOI: 10.1021/acscatal.0c01293

Abstract: This work reports gold-catalyzed highly enantioselective nitroso-Povarov reactions between cyclopentadienes and nitrosoarenes in cold dichloroethane, in which nitrosoarenes serve as 4π-electron don... read more here.

Keywords: catalyzed highly; povarov; povarov reactions; nitroso povarov ... See more keywords
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Iridium-Catalyzed Highly Efficient and Site-Selective Deoxygenation of Alcohols

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Published in 2018 at "ACS Catalysis"

DOI: 10.1021/acscatal.8b02495

Abstract: An iridium-catalyzed, highly efficient, and site-selective deoxygenation of primary, secondary, and tertiary alcohols has been realized, under the assistance of a 4-(N-substituted amino)aryl directing group. Only the hydroxyl adjacent to the directing group can be… read more here.

Keywords: catalyzed highly; site selective; iridium catalyzed; deoxygenation ... See more keywords
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Stretchable chiral pockets for palladium-catalyzed highly chemo- and enantioselective allenylation

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Published in 2021 at "Nature Communications"

DOI: 10.1038/s41467-021-22498-1

Abstract: Pyrazolones are a vital class of heterocycles possessing various biological properties and much attention is paid to the diversified synthesis of enantiopure pyrazolone derivatives. We describe here the development of diphenylphosphinoalkanoic acid based chiral bisphosphine… read more here.

Keywords: catalyzed highly; palladium catalyzed; stretchable chiral; chiral pockets ... See more keywords
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Copper-catalyzed highly selective approach to 2-boroallylic silanes from allenylsilanes

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Published in 2017 at "Organic chemistry frontiers"

DOI: 10.1039/c7qo00135e

Abstract: A highly chemo- and regioselective copper-catalyzed borylcupration of 1,2-allenylsilanes affords 2-borylallylsilanes by applying the ligand effect. Many synthetically attractive functional groups are well tolerated. As demonstrated, such 2-borylallylsilanes are very useful dimetallic reagents in organic… read more here.

Keywords: highly selective; catalyzed highly; selective approach; boroallylic silanes ... See more keywords
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Cobalt-catalyzed highly diastereoselective [3 + 2] carboannulation reactions: facile access to substituted indane derivatives.

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Published in 2022 at "Chemical communications"

DOI: 10.1039/d1cc05245d

Abstract: Efficient oxidative [3 + 2] annulation reaction involving aryl hydrazones and heterobicyclic alkenes has been realized with inexpensive and earth-abundant cobalt salts under aerobic conditions. The reaction proceeds via directing-group-assisted C-H activation and exo-selective migratory… read more here.

Keywords: cobalt catalyzed; diastereoselective carboannulation; carboannulation reactions; highly diastereoselective ... See more keywords
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SnBr2-catalyzed highly selective synthesis of alkyl ethers from monoterpenes

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Published in 2020 at "Comptes Rendus Chimie"

DOI: 10.5802/crchim.11

Abstract: An efficient and Brønsted acid-free route to synthesize monoterpene ethers was developed using SnBr2 as inexpensive and commercially affordable catalyst. This process consists of the synthesis of α-terpinyl alkyl ethers in SnBr2-catalyzed reactions of β-pinene… read more here.

Keywords: highly selective; catalyzed highly; alkyl ethers; snbr2 catalyzed ... See more keywords