C (sp 2)–H cyclobutylation of hydroxyarenes enabled by silver-π-acid catalysis: diastereocontrolled synthesis of 1, 3-difunctionalized cyclobutanes

L Tang, QN Huang, F Wu, Y Xiao, JL Zhou, TT Xu… - Chemical …, 2023 - pubs.rsc.org
Ring-opening of bicyclo [1.1. 0] butanes (BCBs) is emerging as a powerful strategy for 1, 3-
difunctionalized cyclobutane synthesis. However, reported radical strain-release reactions …

The transition-metal-catalyzed stereoselective ring-expansion of vinylaziridines and vinyloxiranes

T Sarkar, K Talukdar, BK Das, TA Shah… - Organic & …, 2021 - pubs.rsc.org
The transition-metal-aided stereoselective construction of sp3-carbon-rich heterocyclic
scaffolds using strained-ring systems has received considerable attention in recent years …

Metal-Catalyzed (4 + 3) Cyclization of Vinyl Aziridines with para-Quinone Methide Derivatives

F Jiang, FR Yuan, LW Jin, GJ Mei, F Shi - ACS Catalysis, 2018 - ACS Publications
The development of (4+ 3) cyclizations of vinyl aziridines, especially catalytic asymmetric
versions, is needed in organic synthesis. This report describes an iridium-catalyzed (4+ 3) …

Unveiling the chemistry and synthetic potential of catalytic cycloaddition reaction of allenes: a review

S Sikandar, AF Zahoor, A Ghaffar, MN Anjum… - Molecules, 2023 - mdpi.com
Allenes with two carbon–carbon double bonds belong to a unique class of unsaturated
hydrocarbons. The central carbon atom of allene is sp hybridized and forms two σ-bonds …

Pd/PC‐Phos‐Catalyzed Enantioselective Intermolecular Denitrogenative Cyclization of Benzotriazoles with Allenes and N‐Allenamides

PC Zhang, J Han, J Zhang - Angewandte Chemie, 2019 - Wiley Online Library
Reported herein is an asymmetric Pd/PC‐Phos‐catalyzed denitrogenative cyclization of
benzotriazoles with allenes and N‐allenamides, representing the first example of …

Cooperative Isothiourea/Iridium-Catalyzed Asymmetric Annulation Reactions of Vinyl Aziridines with Pentafluorophenyl Esters

Q Wang, T Fan, J Song - Organic Letters, 2023 - ACS Publications
Chiral γ-lactam-containing skeletons are important motifs in bioactive natural products,
pharmaceuticals, and bioactive molecules. Herein, we report a general and modular …

Rapid Asymmetric Synthesis of Disubstituted Allenes by Coupling of Flow‐Generated Diazo Compounds and Propargylated Amines

JS Poh, S Makai, T von Keutz, DN Tran… - Angewandte Chemie …, 2017 - Wiley Online Library
We report herein the asymmetric coupling of flow‐generated unstabilized diazo compounds
and propargylated amine derivatives, using a new pyridinebis (imidazoline) ligand, a copper …

Electron-deficient alkynes as dipolarophile in Pd-catalyzed enantioselective (3+ 2) cycloaddition reaction with vinyl cyclopropanes

WP Ding, GP Zhang, YJ Jiang, J Du, XY Liu… - Organic …, 2019 - ACS Publications
The activated alkynes have been used successfully for the first time as the dipolarophile in
the palladium-catalyzed asymmetric (3+ 2) cycloaddition, affording highly functionalized …

A photocatalytic traceless C–N bond formation/cleavage strategy enabling the use of (α-chiral) alkyl aldehydes as deoxygenative (chiral) alkyl radical equivalents

H Bao, L Zheng, Q Liu, M Han, Y Li, M Bao… - Organic Chemistry …, 2023 - pubs.rsc.org
A synthetic idea for the general and efficient utilization of (α-chiral) alkyl aldehydes as
deoxygenative (chiral) alkyl radical equivalents based on a photocatalytic traceless C–N …

Visible-Light Photoredox-Catalyzed Formal [5 + 1] Cycloaddition of N-Tosyl Vinylaziridines with Difluoroalkyl Halides

Y Liu, W Luo, Z Wang, Y Zhao, J Zhao, X Xu… - Organic …, 2020 - ACS Publications
A visible-light photoredox-catalyzed formal [5+ 1] cycloaddition of N-tosyl vinylaziridines with
difluoroalkyl halides as unique C1 synthons was developed. The procedure provides an …