Chemistry of six-membered cyclic oxime ethers. Application in the synthesis of bioactive compounds
AY Sukhorukov, SL Ioffe - Chemical reviews, 2011 - ACS Publications
Interest in the cyclic oxime ethers is due to their high potential for application in the target-
oriented synthesis of naturally occurring and biologically active molecules. 1-9 Five …
oriented synthesis of naturally occurring and biologically active molecules. 1-9 Five …
Recent developments on the chemistry of aliphatic nitro compounds under aqueous medium
R Ballini, L Barboni, F Fringuelli, A Palmieri, F Pizzo… - Green …, 2007 - pubs.rsc.org
Aliphatic nitro derivatives represent an important class of useful molecules in organic
synthesis. The versatility of these compounds is largely due to their easy availability and …
synthesis. The versatility of these compounds is largely due to their easy availability and …
Efficient, direct α-methylenation of carbonyls mediated by diisopropylammonium trifluoroacetate
A Bugarin, KD Jones, BT Connell - Chemical Communications, 2010 - pubs.rsc.org
Efficient, direct α-methylenation of carbonyls mediated by diisopropylammonium trifluoroacetate -
Chemical Communications (RSC Publishing) DOI:10.1039/B924577D Royal Society of Chemistry …
Chemical Communications (RSC Publishing) DOI:10.1039/B924577D Royal Society of Chemistry …
Current developments in Michael addition‐based multicomponent domino reactions involving 1, 3‐dicarbonyls and derivatives
F Liéby‐Muller, C Simon… - QSAR & …, 2006 - Wiley Online Library
The aim of this mini‐review is to present an overview of the high synthetic potential of
Multicomponent Reactions (MCRs) involving the specific reactivity of easily accessible 1, 3 …
Multicomponent Reactions (MCRs) involving the specific reactivity of easily accessible 1, 3 …
Highly Substrate‐Selective Macrocyclic Ring Closing Metathesis
A selective ring‐closing metathesis (RCM) reaction for the formation of large macrocycles by
using latent sulfur chelated ruthenium iodide benzylidenes, readily activated by thermal and …
using latent sulfur chelated ruthenium iodide benzylidenes, readily activated by thermal and …
Water mediated trapping of active methylene intermediates generated by IBX-induced oxidation of Baylis–Hillman adducts with nucleophiles
Water proved to be an efficient solvent for oxidation of a Baylis–Hillman adduct with IBX. The
generated product, a methylene intermediate, could be trapped in situ by many nucleophiles …
generated product, a methylene intermediate, could be trapped in situ by many nucleophiles …
Zinc oxide nanoparticles as efficient catalyst for the synthesis of novel di-spiroindolizidine bisoxindoles in aqueous medium
N Satish Kumar, MS Reddy, VR Bheeram… - Environmental …, 2019 - Springer
Developing environmentally benign synthetic protocols such as reaction in water is a major
challenge. However, many of the known methods carried out in an aqueous medium are not …
challenge. However, many of the known methods carried out in an aqueous medium are not …
Highly efficient regio and diastereoselective synthesis of functionalized bis-spirooxindoles and their antibacterial properties
A simple, efficient, regioselective and diastereoselective method has been developed for the
synthesis of diversely functionalized spirooxindole-pyrrolidines using 0.5 mol% of ceric …
synthesis of diversely functionalized spirooxindole-pyrrolidines using 0.5 mol% of ceric …
Polystyryl‐BEMP as an Efficient Recyclable Catalyst for the Nucleophilic Addition of Nitroalkanes to α, β‐Unsaturated Carbonyl Compounds under Solvent‐Free …
R Ballini, L Barboni, L Castrica… - Advanced Synthesis …, 2008 - Wiley Online Library
tert‐Butylimino‐2‐diethylamino‐1, 3‐dimethylperhydro‐1, 3, 2‐diazaphosphorine supported
on polystyrene (PS‐BEMP) is an efficient catalyst for the addition of nitroalkanes (1–1.5 …
on polystyrene (PS‐BEMP) is an efficient catalyst for the addition of nitroalkanes (1–1.5 …
β-Diketo building blocks for MCRs-based syntheses of heterocycles
MMS del Duque, C Allais, N Isambert… - … of Heterocycles via …, 2010 - Springer
In the context of sustainable chemistry, because of economic and ecological increasing
pressure, domino multicomponent reactions (MCRs) constitute a central academic and …
pressure, domino multicomponent reactions (MCRs) constitute a central academic and …