Borrowing hydrogen is a process that is used to diversify the synthetic utility of commodity
alcohols. A catalyst first oxidizes an alcohol by removing hydrogen to form a reactive …

Direct substitution of readily available alcohols is recognized as a key research area in
green chemical synthesis. Starting from simple racemic secondary alcohols, the …

The combination of nickel metallaphotoredox catalysis, hydrogen atom transfer catalysis,
and a Lewis acid activation mode, has led to the development of an arylation method for the …

A homogeneous manganese‐catalyzed cross‐coupling of two secondary alcohols for the
divergent synthesis of γ‐disubstituted alcohols and β‐disubstituted ketones is reported …

The α-alkylation of ketones using an earth-abundant and nonprecious NiBr 2/L1 system is
reported. This nickel-catalyzed reaction could be performed in gram scale and successfully …

Herein we disclose a series of phosphine-free cobalt (II)-based catalytic systems bearing a
redox non-innocent amine functionalized azo-aromatic pincer-like ligand for the synthesis of …

This study reports a nickel-catalyzed sustainable synthesis of polysubstituted quinolines
from α-2-aminoaryl alcohols by a sequential dehydrogenation and condensation process …

Herein, a phosphine-free pincer ruthenium (III) catalyzed β-alkylation of secondary alcohols
with primary alcohols to α-alkylated ketones and two different secondary alcohols to β …

Herein, an unprecedented ruthenium (II) catalyzed direct cross-coupling of two different
secondary alcohols to β-disubstituted ketones is reported. Cyclic, acylic, symmetrical, and …

A BINAP-Cu system supported by hydrotalcite has been developed and proved to be a
highly efficient catalyst for the atom-efficient and green borrowing hydrogen reaction and …