Nickel chain-walking catalysis: a journey to migratory carboboration of alkenes
Y Li, G Yin - Accounts of Chemical Research, 2023 - ACS Publications
Conspectus Chain-walking offers extensive opportunities for innovating synthetic methods
that involve constructing chemical bonds at unconventional sites. This approach provides …
that involve constructing chemical bonds at unconventional sites. This approach provides …
Difunctionalization of alkenes involving metal migration
The direct difunctionalization of alkenes, a cheap and abundant feedstock, represents one of
the most attractive strategies for increasing molecular complexity in synthetic organic …
the most attractive strategies for increasing molecular complexity in synthetic organic …
Enantioselective reductive cross-couplings of olefins by merging electrochemistry with nickel catalysis
YZ Wang, B Sun, XY Zhu, YC Gu, C Ma… - Journal of the American …, 2023 - ACS Publications
The merger of electrochemistry and transition metal catalysis has emerged as a powerful
tool to join two electrophiles in an enantioselective manner. However, the development of …
tool to join two electrophiles in an enantioselective manner. However, the development of …
Nickel-catalyzed regio-and enantioselective borylative coupling of terminal alkenes with alkyl halides enabled by an anionic bisoxazoline ligand
Z Li, H Shi, X Chen, L Peng, Y Li… - Journal of the American …, 2023 - ACS Publications
Chiral boronic esters are a class of versatile building blocks. We describe herein an
asymmetric nickel-catalyzed borylative coupling of terminal alkenes with nonactivated alkyl …
asymmetric nickel-catalyzed borylative coupling of terminal alkenes with nonactivated alkyl …
Nickel-catalyzed enantioconvergent reductive hydroalkylation of olefins with α-heteroatom phosphorus or sulfur alkyl electrophiles
SJ He, JW Wang, Y Li, ZY Xu, XX Wang… - Journal of the …, 2019 - ACS Publications
Substantial advances in enantioconvergent C (sp3)–C (sp3) bond formation reactions have
been made in recent years through the use of transition-metal-catalyzed cross-coupling …
been made in recent years through the use of transition-metal-catalyzed cross-coupling …
Modular access to substituted cyclohexanes with kinetic stereocontrol
Substituted six-membered cyclic hydrocarbons are common constituents of biologically
active compounds. Although methods for the synthesis of thermodynamically favored …
active compounds. Although methods for the synthesis of thermodynamically favored …
Walking metals: catalytic difunctionalization of alkenes at nonclassical sites
Migration of metals along a carbon chain is triggered by two of the most common
organometallic elementary steps–β-hydride (β-H) elimination and alkene hydrometallation …
organometallic elementary steps–β-hydride (β-H) elimination and alkene hydrometallation …
Catalyst-controlled enantioselective 1, 1-arylboration of unactivated olefins
W Wang, C Ding, G Yin - Nature Catalysis, 2020 - nature.com
Enantioselective difunctionalization of alkenes constitutes an efficient strategy to assemble
complex chiral molecules from simple racemic or achiral starting materials. Here we present …
complex chiral molecules from simple racemic or achiral starting materials. Here we present …
Nickel-catalyzed 1, 1-aminoborylation of unactivated terminal alkenes
L Talavera, RRA Freund, H Zhang, M Wakeling… - ACS …, 2023 - ACS Publications
Herein, we disclose a Ni-catalyzed 1, 1-difunctionalization of unactivated terminal alkenes
that enables the incorporation of two different heteroatom motifs across an olefin backbone …
that enables the incorporation of two different heteroatom motifs across an olefin backbone …
Regio-and enantioselective remote hydroarylation using a ligand-relay strategy
Y He, J Ma, H Song, Y Zhang, Y Liang, Y Wang… - Nature …, 2022 - nature.com
The design of a single complicated chiral ligand to well-promote each step of an asymmetric
cascade reaction is sometimes a formidable challenge in transition metal catalysis. In this …
cascade reaction is sometimes a formidable challenge in transition metal catalysis. In this …