The carbon–carbon (C–C) bond cleavage of cyclopropanols is a wide area of research with
much current activity. This review highlights new developments in this area over the past two …

Recent developments in the stereoselective synthesis of polysubstituted cyclopropanes
nowadays allow chemists to easily access these strained rings with high diastereo-and …

Catalytic enantioselective functionalization of cyclobutenes constitutes a general and
modular strategy for construction of enantioenriched complex cyclobutanes bearing multiple …

Visible light induced singlet nucleophilic carbenes undergo rapid [2+ 1]-cycloaddition with
tethered olefins to afford unique bicyclo [3.1. 0] hexane and bicyclo [4.1. 0] heptane …

Conspectus The pursuit of novel and eco-friendly methods in organic synthesis is gaining
prominence, with a strong emphasis on green transformations using renewable and …

β2-Amino carbonyls, an α-substituted β-amino scaffold, hold a prominent place in the
development of new pharmaceuticals and peptidomimetics. Herein, we report a highly …

We report the difunctionalization of unactivated, terminal olefins through intermolecular
addition of α-bromoketones,-esters, and-nitriles followed by formation of 4-to 6-membered …

We report here a homo‐Mannich reaction of cyclopropanol with an iminium ion, generated
by an asymmetric allylic dearomatization of indole, to construct a tricyclic hydrocarbazole …

The ring opening of cyclopropanols is rarely used in multicomponent reactions. Herein we
report the three-component reaction of cyclopropanols with alkenes and tert-butyl …

We report herein an enantioselective conjugate addition reaction of a zinc homoenolate,
catalytically generated via ring opening of a cyclopropanol, to an α, β-unsaturated ketone …