Palladium-Catalyzed Synthesis of 2-(1-Isochromen-3-yl)acetalde-hydes via Carboxyl-Directed C(sp2)—H Alkylation/Annulation DOI
Yue Wang,

Xuyan Yang,

Tianyu Liu

и другие.

Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(11), С. 3556 - 3556

Опубликована: Янв. 1, 2024

Язык: Английский

Ether-Directed Enantioselective C(sp2)–H Borylation for the Synthesis of Axially Chiral Biaryls DOI

Changji Liu,

Chengcai Xia,

Shu‐Yong Song

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Апрель 9, 2025

We report an ether-directed enantioselective C(sp2)-H borylation catalyzed by a chiral bidentate boryl ligand (CBL)/iridium system for constructing axially biaryls. This method delivered diverse biaryls with good to high enantioselectivities, accommodating varied electronic and steric substituents on the aryl rings. Gram-scale synthesis downstream transformations of C-B bond underscored its practicality.

Язык: Английский

Процитировано

0

Synthesis of Axially Chiral Compounds via Transition Metal-Catalyzed Atroposelective C–H Functionalization DOI
Gang Liao, Bing‐Feng Shi

Accounts of Chemical Research, Год журнала: 2025, Номер unknown

Опубликована: Апрель 14, 2025

ConspectusAxially chiral skeletons are prevalent in natural products and biologically important compounds, they widely utilized as privileged scaffolds enantioselective catalysis. Consequently, the catalytic atroposelective synthesis of enantiopure atropisomers has garnered considerable attention. A variety synthetic strategies involving metal catalysis or organocatalysis have been developed. Among these elegant approaches, transition metal-catalyzed C-H activation emerged an atom- step-economical strategy to streamline construction axially compounds recent years.In this Account, we discuss our efforts different types including biaryls, atropisomeric styrenes, C-N atropisomers, via strategies. To end, developed several transient directing group (cTDG) using Pd(OAc)2 tert-leucine (Tle), well systems Pd(II)/chiral phosphoric acid (CPA), Pd(II)/l-pyroglutamic (pGlu), Pd(0)/norbornene cooperative with a biimidazoline (BiIM) ligand, Co(II)/salicyloxazoline (Salox).At outset, successfully applied cTDG access biaryl aldehydes through Pd-catalyzed olefination, alkynylation, allylation, naphthylation, alkylation. The efficacy methods demonstrated aldehyde catalysts products, such TAN-1085, (+)-isochizandrin, (+)-steganone. facilitate diverse functionalities, novel Pd(II)/CPA system, which enables preparation various quinolines, biaryl-2-amines, biaryls bearing chalcogenoether units high enantioselectivities. system also allows for more challenging conjugated diene-based styrenes.Nonbiaryl styrenes anilides, present challenges due their conformational instability higher degree rotational freedom compared counterparts. We addressed achieved highly efficient anilides Pd(II)/pGlu Pd(0)/norbornene/BiIM In addition palladium catalysis, cobalt(II)/Salox vicinal C-C stereogenic axes, remote distinct diaxes, calix[4]arenes featuring both inherent axial chirality. anticipate that will find broad applications synthetically useful compounds.

Язык: Английский

Процитировано

0

Palladium-Catalyzed Synthesis of 2-(1-Isochromen-3-yl)acetalde-hydes via Carboxyl-Directed C(sp2)—H Alkylation/Annulation DOI
Yue Wang,

Xuyan Yang,

Tianyu Liu

и другие.

Chinese Journal of Organic Chemistry, Год журнала: 2024, Номер 44(11), С. 3556 - 3556

Опубликована: Янв. 1, 2024

Язык: Английский

Процитировано

0