Ruthenium and Rhodium‐Catalyzed Carbonylation Reactions

XF Wu, H Neumann - ChemCatChem, 2012 - Wiley Online Library
Over the last few decades, carbonylation reactions have been accepted as important
chemical transformations for both academic and industrial research. Carboxylic acid …

Nickel-catalysed regio-and stereoselective acylzincation of unsaturated hydrocarbons with organozincs and CO

Y Weng, Y Zhang, A Turlik, X Wu, H Li, F Fei, Y Yao… - Nature …, 2023 - nature.com
Carbometallation of unsaturated hydrocarbons is one of the most straightforward
functionalizations of carbon–carbon unsaturated bonds; however, the analogous …

Advances in nucleophilic allylic fluorination

AM Sorlin, FO Usman, CK English, HM Nguyen - ACS Catalysis, 2020 - ACS Publications
Numerous procedures focus on inserting the fluorine atom into the carbon frameworks of
synthetically useful target molecules using various nucleophilic fluorinating reagents …

Boron reagents and catalysts for the functionalization of strained heterocycles

M Pineschi - Advanced Synthesis & Catalysis, 2021 - Wiley Online Library
The particular nature of boron compounds allows an ample modularity of their properties
ranging from Lewis acids, C‐nucleophiles, B‐nucleophiles, or even conjunctive reagents for …

Rh (III)-catalyzed C–H activation–desymmetrization of diazabicycles with arenes: facile synthesis of functionalized cyclopentenes

Y Zhang, Q Wu, S Cui - Chemical Science, 2014 - pubs.rsc.org
A Rh (III)-catalyzed C–H activation–desymmetrization of diazabicycles with arenes as an
expedient approach to functionalized cyclopentenes is reported. This protocol provides a …

The First General and Selective Palladium (II)‐Catalyzed Alkoxycarbonylation of Arylboronates: Interplay among Benzoquinone‐Ligated Palladium (0) Complex …

Y Yamamoto - Advanced Synthesis & Catalysis, 2010 - Wiley Online Library
Methoxycarbonylation of aryl‐and alkenylboron compounds was performed using the
palladium (II) acetate/triphenylphosphine [Pd (OAc) 2/PPh3] catalyst with p‐benzoquinone …

Rhodium catalyzed oxidative coupling of salicylaldehydes with diazabicyclic olefins: a one pot strategy involving aldehyde C–H cleavage and π-allyl chemistry …

E Jijy, P Prakash, M Shimi, PM Pihko… - Chemical …, 2013 - pubs.rsc.org
An efficient one pot strategy for the synthesis of cyclopentene fused chromanone derivatives
through the direct oxidative coupling of salicylaldehydes with bicyclic olefins in the presence …

Palladium Catalyzed Tandem Ring Opening− Ring Closing Reaction of Diazabicyclic Alkenes: A Facile One Pot Strategy for Cyclopentannulation of Heterocycles

J John, IU, E Suresh… - Journal of the American …, 2009 - ACS Publications
A novel palladium catalyzed protocol for the synthesis of cyclopentene fused heterocycles
from diazabicyclic alkenes and ortho-functionalized aryliodides has been elaborated. The …

Stereoselective transformations of meso bicyclic hydrazines: versatile access to functionalized aminocyclopentanes

C Bournaud, F Chung, AP Luna, M Pasco, G Errasti… - …, 2009 - thieme-connect.com
Bicyclic hydrazines, prepared by cycloaddition of cyclopentadiene and diazo compounds,
have great synthetic potential. Numerous asymmetric transformations of these building …

Progress in Transition Metal-Catalyzed Asymmetric Ring-Opening Reactions of Azabicyclic Alkenes

H Cheng, X Liang, X Li, Y Long… - Chinese Journal of Organic …, 2012 - sioc-journal.cn
The recent progress in transition metal-catalyzed ring-opening reactions of azabicyclic
alkenes was reviewed focused on the influence of the types of transition metal catalysts …