2, 5-Diketopiperazines: synthesis, reactions, medicinal chemistry, and bioactive natural products

AD Borthwick - Chemical reviews, 2012 - ACS Publications
2, 5-Diketopiperazines (2, 5-DKPs) are cyclodipeptides obtained by the condensation of two
α-amino acids. They not only abound in nature but are often produced as degradation …

3-Substituted-3-hydroxy-2-oxindole, an emerging new scaffold for drug discovery with potential anti-cancer and other biological activities

S Peddibhotla - Current Bioactive Compounds, 2009 - ingentaconnect.com
Natural products and small molecules inspired by them are enjoying a resurgence of interest
because they intersect biological space effectively and selectively. On account of their …

Recent Advances in Palladium‐Catalyzed Cascade Cyclizations

T Vlaar, E Ruijter, RVA Orru - Advanced Synthesis & Catalysis, 2011 - Wiley Online Library
The importance of palladium‐catalyzed cross coupling reactions in contemporary organic
synthesis is undisputed and underlined by the Nobel Prize for Chemistry in 2010. In addition …

Enantioselective organocatalytic aldol reaction using small organic molecules

V Bisai, A Bisai, VK Singh - Tetrahedron, 2012 - Elsevier
Enantioselective reactions catalyzed by small organic molecules (asymmetric
organocatalysis) have emerged as one of the most elegant cutting-edge strategies of …

Lewis acid-catalyzed enantioselective hydroxylation reactions of oxindoles and β-keto esters using DBFOX ligand

T Ishimaru, N Shibata, J Nagai… - Journal of the …, 2006 - ACS Publications
The first catalytic enantioselective hydroxylation reaction of both 3-aryl and 3-alkyl-2-
oxindoles using the DBFOX− Zn (II) complex, leading to pharmaceutically important chiral 3 …

Catalytic asymmetric hydroxylation of oxindoles by molecular oxygen using a phase-transfer catalyst

D Sano, K Nagata, T Itoh - Organic Letters, 2008 - ACS Publications
The highly enantioselective catalytic hydroxylation of 3-substituted oxindoles was achieved
by using a phase-transfer catalyst with molecular oxygen as an oxidant. The product then …

Catalytic asymmetric synthesis of 3-hydroxyoxindole: a potentially bioactive molecule

A Kumar, SS Chimni - RSC advances, 2012 - pubs.rsc.org
The recent emergence of biological activities of chiral 3-substituted-3-hydroxy-2-oxindoles
has inspired synthetic chemists to develop new methodologies for their synthesis. Both …

Organocatalytic asymmetric aldol reaction of ketones with isatins: straightforward stereoselective synthesis of 3-alkyl-3-hydroxyindolin-2-ones

JR Chen, XP Liu, XY Zhu, L Li, YF Qiao, JM Zhang… - Tetrahedron, 2007 - Elsevier
An efficient asymmetric aldol condensation of ketones with isatins has been developed
using an l-proline-derived bifunctional organocatalyst. This strategy allows the …

Facile and One-Pot Access of 3,3-Bis(indol-3-yl)indolin-2-ones and 2,2-Bis(indol-3-yl)acenaphthylen-1(2H)-one Derivatives via an Eco-Friendly Pseudo …

G Brahmachari, B Banerjee - ACS Sustainable Chemistry & …, 2014 - ACS Publications
A simple, straightforward, and highly efficient pseudo-three-component one-pot synthesis of
a series of pharmaceutically interesting functionalized 3, 3-bis (indol-3-yl) indolin-2-ones (3a …

Metal-free iodine-catalyzed synthesis of fully substituted pyrazoles and its sulphenylation

J Sun, JK Qiu, YL Zhu, C Guo, WJ Hao… - The Journal of …, 2015 - ACS Publications
A direct and metal-free access toward fully substituted pyrazoles and its sulphenylation has
been established through an iodine-mediated three-component [3+ 2] annulation of β …