A General Organocatalytic Enantioselective Malonate Addition to α, β‐Unsaturated Enones

V Wascholowski, KR Knudsen… - … A European Journal, 2008 - Wiley Online Library
A general enantioselective organocatalytic conjugate addition procedure of a variety of
malonates to α, β‐unsaturated enone systems is presented. The reaction is efficiently …

The Krapcho Dealkoxycarbonylation Reaction of Esters with α‐Electron‐Withdrawing Substituents

A Paul Krapcho, E Ciganek - Organic Reactions, 2004 - Wiley Online Library
The Krapcho reaction involves esters with α‐electron‐withdrawing substituents such as
malonates, β‐keto esters, and α‐cyano esters, which undergo dealkoxycarbonylation on …

Direct oxidation of bromo-derived Fischer–Borsche oxo-ring using molecular iodine with combined experimental and computational study

VT Humne, MH Ghom, MS Naykode… - Organic & …, 2022 - pubs.rsc.org
A direct oxidation of the bromo-derived Fischer–Borsche oxo-ring leading to
carbazolequinone has been developed by using molecular iodine. This unprecedented …

In situ formed acetals facilitated direct Michael addition of unactivated ketones

SR Koppolu, R Balamurugan - New Journal of Chemistry, 2017 - pubs.rsc.org
TfOH-promoted synthesis of 1, 5-diketones by the Michael reaction of unactivated ketones
with chalcones has been described. Acetals formed under HC (OMe) 3/TfOH conditions …

A novel transformation of β-1, 2, 3-thiadiazol-5-yl enamines into thieno [2, 3-d] pyridazines

Y Rozin, S Zhidovinov, T Beryozkina, Y Shafran… - Tetrahedron …, 2015 - Elsevier
Abstract Reactions of β-1, 2, 3-thiadiazol-5-yl enamines with acetyl chloride in 1, 4-dioxane
lead to the formation of either dienamines or novel thieno [2, 3-d] pyridazines depending on …

Efficient synthesis of highly functionalized vinylogous thiol esters

J Liu, X Xu, D Li, L Zhang, K Zhang, Q Liu - Tetrahedron Letters, 2010 - Elsevier
A series of vinylogous thiol esters 2, 3 and 2, 6-dioxo-1, 2, 5, 6-tetrahydropyridines (cyclic
vinylogous thiol esters) 4 were prepared in high to excellent yields from the tandem reaction …

Iodine‐Catalyzed Aerobic Oxidative Cleavage of C–C δ‐Bonds: Difunctionalization of Dienones

KX Feng, QY Shen, AB Xia, X Zhang… - European Journal of …, 2020 - Wiley Online Library
A new and efficient catalytic strategy that combines organocatalysis and iodine catalysis was
first developed for the difunctionalization of dienone. The reaction proceeds under metal …

II. Discovery of a novel series of CXCR3 antagonists with a beta amino acid core

I Bata, Z Tömösközi, P Buzder-Lantos, A Vasas… - Bioorganic & Medicinal …, 2016 - Elsevier
A new series of beta amino acids, which act as CXCR3 antagonists, has been identified. The
formerly optimized N, N-disubstituted benzylamine derivatives with carboxylic acid function …

Acid-promoted SN1/E1 fragmentation/dimerization of 2-cumylmalonates

JT Reeves, DR Fandrick, Z Tan, JJ Song, NK Yee… - Tetrahedron …, 2009 - Elsevier
Several diethyl 2-cumylmalonates underwent fragmentation and dimerization in PPA at
elevated temperatures to give 1, 1, 3-trimethyl-3-arylindanes in good yields. The same …