Arylglyoxals in synthesis of heterocyclic compounds

B Eftekhari-Sis, M Zirak, A Akbari - Chemical reviews, 2013 - ACS Publications
Heterocycles are an extraordinarily important class of compounds, making up more than half
of all known organic compounds. Heterocycles are present in a wide variety of drugs, most …

Applications of allylamines for the syntheses of aza-heterocycles

S Nag, S Batra - Tetrahedron, 2011 - Elsevier
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Stereoselective syntheses and transformations of chiral 1, 3-aminoalcohols and 1, 3-diols derived from nopinone

Z Szakonyi, T Gonda, SB Oetvoes, F Fueloep - Tetrahedron: Asymmetry, 2014 - Elsevier
Abstract A library of 1, 3-difunctionalized pinane derivatives were synthesized and applied
as chiral catalysts in the addition of diethylzinc to benzaldehyde. 1, 3-Aminoalcohol 6a was …

Highly Homogeneous Stereocontrolled Construction of Quaternary Hydroxyesters by Addition of Dimethylzinc to α‐Ketoesters Promoted by Chiral …

R Infante, J Nieto, C Andres - Chemistry–A European Journal, 2012 - Wiley Online Library
A highly efficient enantioselective addition of Me2Zn to α‐ketoesters, assisted by a chiral
perhydro‐1, 3‐benzoxazine ligand, is described. This novel catalytic system offers …

Divergent Synthesis, Antiproliferative and Antimicrobial Studies of 1, 3‐Aminoalcohol and 3‐Amino‐1, 2‐Diol Based Diaminopyrimidines

M Raji, TM Le, T Huynh, A Szekeres… - Chemistry & …, 2022 - Wiley Online Library
A series of novel diaminopyrimidines containing pinane moieties were synthesized via an
efficient methodology starting from pinane‐based aminoalcohols, aminodiols and 2, 4 …

Perhydro-1, 3-benzoxazines derived from (−)-8-aminomenthol as ligands for the catalytic enantioselective addition of diethylzinc to aldehydes

C Andrés, R Infante, J Nieto - Tetrahedron: Asymmetry, 2010 - Elsevier
The catalytic potency of a series of perhydro-1, 3-benzoxazines prepared from (−)-8-
aminomenthol was examined in the enantioselective addition of diethylzinc to aldehydes …

Asymmetric additive-free aryl addition to aldehydes using perhydrobenzoxazines as ligands and boroxins as aryl source

R Infante, J Nieto, C Andrés - Organic & Biomolecular Chemistry, 2011 - pubs.rsc.org
A highly efficient enantioselective aryl addition to aldehydes using boroxins as aryl source
and conformationally restricted perhydro-1, 3-benzoxazines as ligands is reported. Both …

Enantioselective synthesis of 3-hydroxy-and 3-amino-3-alkynyl-2-oxindoles by the dimethylzinc-mediated addition of terminal alkynes to isatins and isatin-derived …

E Prieto, JD Martín, J Nieto, C Andrés - Organic & Biomolecular …, 2023 - pubs.rsc.org
A common protocol for enantioselective alkynylation of isatins and isatin-derived ketimines
using terminal alkynes and Me2Zn in the presence of a catalytic amount of a chiral perhydro …

Enantiocontrolled Synthesis of Tertiary α‐Hydroxy‐α‐ynyl Esters by Dimethylzinc‐Mediated Addition of Alkynes to α‐Keto Esters

R Infante, A Gago, J Nieto… - Advanced Synthesis & …, 2012 - Wiley Online Library
Abstract A perhydro‐1, 3‐benzoxazine behaves as an excellent chiral ligand in the
nucleophilic addition of alkynylzinc derivatives, prepared from terminal alkynes and …

Stereoselective synthesis and cytoselective toxicity of monoterpene-fused 2-imino-1, 3-thiazines

Z Szakonyi, I Zupkó, R Sillanpää, F Fülöp - Molecules, 2014 - mdpi.com
Starting from pinane-, apopinane-and carane-based 1, 3-amino alcohols obtained from
monoterpene-based β-amino acids, a library of monoterpene-fused 2-imino-1, 3-thiazines …