Bifunctional amine‐squaramides: powerful hydrogen‐bonding organocatalysts for asymmetric domino/cascade reactions

P Chauhan, S Mahajan, U Kaya… - … Synthesis & Catalysis, 2015 - Wiley Online Library
Organocatalytic domino/cascade reactions provide a convenient method for the construction
of complex molecular structures bearing multiple stereocenters in a highly stereoselective …

Squaramide‐catalyzed asymmetric reactions

BL Zhao, JH Li, DM Du - The Chemical Record, 2017 - Wiley Online Library
Bifunctional squaramides have emerged as powerful hydrogen‐bonding catalysts for
promoting a wide array of useful asymmetric reactions, which provides convenient methods …

Cobalt-catalyzed diastereo-and enantioselective carbon–carbon bond forming reactions of cyclobutenes

Z Liang, L Wang, Y Wang, L Wang… - Journal of the …, 2023 - ACS Publications
Catalytic enantioselective functionalization of cyclobutenes constitutes a general and
modular strategy for construction of enantioenriched complex cyclobutanes bearing multiple …

Recent Advances in Organocatalytic Methods for Asymmetric C C Bond Formation

U Scheffler, R Mahrwald - Chemistry–A European Journal, 2013 - Wiley Online Library
Beyond a doubt organocatalysis belongs to the most exciting and innovative chapters of
organic chemistry today. Organocatalysis has emerged not only as a complement to metal …

Squaramide equilibrium acidities in DMSO

X Ni, X Li, Z Wang, JP Cheng - Organic letters, 2014 - ACS Publications
A number of popular squaramide organocatalysts' acidities were determined by an
overlapping indicator method in DMSO via UV spectrophotometric titrations. The p K a …

Construction of vicinal tertiary and all-carbon quaternary stereocenters via Ir-catalyzed regio-, diastereo-, and enantioselective allylic alkylation and applications in …

WB Liu, CM Reeves, SC Virgil… - Journal of the American …, 2013 - ACS Publications
Highly congested vicinal stereocenters comprised of tertiary and all-carbon quaternary
centers were generated via Ir-catalyzed asymmetric allylic alkylation of β-ketoesters. These …

Enantioselective Organocatalytic Four‐Atom Ring Expansion of Cyclobutanones: Synthesis of Benzazocinones

Y Zhou, YL Wei, J Rodriguez… - Angewandte Chemie, 2019 - Wiley Online Library
An enantioselective Michael addition–four‐atom ring expansion cascade reaction involving
cyclobutanones activated by a N‐aryl secondary amide group and ortho‐amino …

Iridium‐Catalyzed Enantioselective C(sp3)–H Borylation of Cyclobutanes

X Chen, L Chen, H Zhao, Q Gao… - Chinese Journal of …, 2020 - Wiley Online Library
Summary of main observation and conclusion We herein report the first example of iridium‐
catalyzed enantioselective C (sp3)–H borylation of cyclobutanes using benzoxazoline as the …

Stereocontrolled synthesis and functionalization of cyclobutanes and cyclobutanones

F Secci, A Frongia, PP Piras - Molecules, 2013 - mdpi.com
In the last decade a certain number of new cyclobutane and cyclobutanone synthesis and
functionalization protocols have been published. Organo-and biocatalyzed eco-friendly …

[HTML][HTML] Enantioselective construction of α-quaternary cyclobutanones by catalytic asymmetric allylic alkylation

CM Reeves, C Eidamshaus, J Kim… - … Chemie (International ed …, 2013 - ncbi.nlm.nih.gov
Abstract No Strain, No Gain! The first transition metal-catalyzed enantioselective α-alkylation
of cyclobutanones is reported. This method employs palladium catalysis and an electron …