Catalytic Asymmetric Synthesis of β-Amino α-Tertiary Alcohol through Borrowing Hydrogen Amination DOI
Shahida Perveen, Tariq Ali, Talat S. Rahman

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Март 6, 2025

The first enantioconvergent transition-metal-catalyzed amination of racemic α-tertiary 1,2-diols providing access to vicinal β-amino alcohols is disclosed. iridium-catalyzed reaction proceeds through a chiral phosphoric acid-mediated borrowing hydrogen pathway with excellent yields and enantioselectivities for range amine nucleophiles 1,2-diols. An array were obtained high (50 examples up 91% yield 99% ee). These important amino alcohol products can be easily converted into ligands bioactive skeletons. Mechanistic investigations proposed dynamic kinetic resolution involving imine formation then reduction as the enantiodetermining step.

Язык: Английский

Direct C(sp3)-H functionalization with aryl and alkyl radicals as intermolecular hydrogen atom transfer (HAT) agents DOI
Jia‐Lin Tu, Binbin Huang

Chemical Communications, Год журнала: 2024, Номер unknown

Опубликована: Янв. 1, 2024

Recent years have witnessed the emergence of direct intermolecular C(sp

Язык: Английский

Процитировано

6

Visible-light-driven asymmetric aldol reaction of ketones and glycinates via synergistic Lewis acid/photoredox catalysis DOI Creative Commons
Jiuqi Tan, Longqing Yang,

Hanyu Su

и другие.

Chemical Science, Год журнала: 2024, Номер 15(39), С. 16050 - 16058

Опубликована: Янв. 1, 2024

We have synthesized β-diaryl-β-hydroxyl-α-amino acid derivatives through radical addition-type aldol reaction, which was confirmed by spectroscopic experiments, control and DFT calculations.

Язык: Английский

Процитировано

4

Catalytic Asymmetric Synthesis of β-Amino α-Tertiary Alcohol through Borrowing Hydrogen Amination DOI
Shahida Perveen, Tariq Ali, Talat S. Rahman

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Март 6, 2025

The first enantioconvergent transition-metal-catalyzed amination of racemic α-tertiary 1,2-diols providing access to vicinal β-amino alcohols is disclosed. iridium-catalyzed reaction proceeds through a chiral phosphoric acid-mediated borrowing hydrogen pathway with excellent yields and enantioselectivities for range amine nucleophiles 1,2-diols. An array were obtained high (50 examples up 91% yield 99% ee). These important amino alcohol products can be easily converted into ligands bioactive skeletons. Mechanistic investigations proposed dynamic kinetic resolution involving imine formation then reduction as the enantiodetermining step.

Язык: Английский

Процитировано

0