Late transition metal-catalyzed hydroamination and hydroamidation

L Huang, M Arndt, K Gooßen, H Heydt… - Chemical …, 2015 - ACS Publications
This Review examines recent developments in late transition metal-catalyzed
hydroamination and-amidation reactions. A hydroamination is a reaction in which an N− H …

C–C bond cleavages of cyclopropenes: operating for selective ring-opening reactions

R Vicente - Chemical Reviews, 2020 - ACS Publications
This review highlights key reactivities relying on C–C bond cleavages of cyclopropenes.
Metal-catalyzed and metal-free transformations are covered in reactions involving direct ring …

Hydroamination: direct addition of amines to alkenes and alkynes

TE Muller, KC Hultzsch, M Yus, F Foubelo… - Chemical …, 2008 - ACS Publications
Nitrogen-containing compounds, such as amines, enamines, and imines, are valuable and
commercially important bulk chemicals, specialty chemicals, and pharmaceuticals. 1 Among …

Transition metal chemistry of cyclopropenes and cyclopropanes

M Rubin, M Rubina, V Gevorgyan - Chemical reviews, 2007 - ACS Publications
Three-membered carbocycles are extremely important versatile building blocks for organic
chemistry. Their unique structural and electronic properties give rise to an array of very …

Copper (I)‐Catalyzed Asymmetric Hydrophosphination of 3, 3‐Disubstituted Cyclopropenes

S Zhang, N Jiang, JZ Xiao, GQ Lin… - Angewandte Chemie …, 2023 - Wiley Online Library
Abstract Herein, a copper (I)‐catalyzed asymmetric hydrophosphination of 3, 3‐disubstituted
cyclopropenes is reported. It provides a series of phosphine derivatives in high to excellent …

Synthesis of Chiral Aminocyclopropanes by Rare‐Earth‐Metal‐Catalyzed Cyclopropene Hydroamination

HL Teng, Y Luo, B Wang, L Zhang… - Angewandte …, 2016 - Wiley Online Library
The search for efficient and selective routes for the synthesis of chiral aminocyclopropane
derivatives is of great interest and importance as these structures are important components …

One-pot synthesis of symmetrical and unsymmetrical aryl sulfides by Pd-catalyzed couplings of aryl halides and thioacetates

N Park, K Park, M Jang, S Lee - The Journal of Organic Chemistry, 2011 - ACS Publications
Aryl sulfides were obtained from the coupling reaction of S-aryl (or S-alkyl) thioacetates and
aryl bromides in the presence of palladium catalyst. This reaction method enables the one …

Enantioselective hydrothiolation: diverging cyclopropenes through ligand control

S Nie, A Lu, EL Kuker, VM Dong - Journal of the American …, 2021 - ACS Publications
In this article, we advance Rh-catalyzed hydrothiolation through the divergent reactivity of
cyclopropenes. Cyclopropenes undergo hydrothiolation to provide cyclopropyl sulfides or …

2, 3, 4-or 2, 3, 5-Trisubstituted furans: catalyst-controlled highly regioselective ring-opening cycloisomerization reaction of cyclopropenyl ketones

S Ma, J Zhang - Journal of the American Chemical Society, 2003 - ACS Publications
2, 3, 4-or 2, 3, 5-trisubstituted furans were highly regioselectively formed from the
cycloisomerization reaction of the same starting cyclopropenes 1 via the subtle choice of the …

Highly Enantioselective Rh2(S-DOSP)4-Catalyzed Cyclopropenation of Alkynes with Styryldiazoacetates

JF Briones, J Hansen, KI Hardcastle… - Journal of the …, 2010 - ACS Publications
Dirhodium tetrakis ((S)-N-(dodecylbenzenesulfonyl) prolinate)(Rh2 (S-DOSP) 4) is an
effective catalyst for highly enantioselective cyclopropenation reactions between terminal …