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 …

Glycerol ether synthesis: A bench test for green chemistry concepts and technologies

M Sutter, ED Silva, N Duguet, Y Raoul, E Métay… - Chemical …, 2015 - ACS Publications
Naturally occurring, glycerol ethers are generally pure enantiomers, and batylic, chimylic,
and selachylic alcohols (Scheme 1) are the major ones which can be found in lipid …

Epihalohydrins in organic synthesis

GS Singh, K Mollet, M D'hooghe… - Chemical Reviews, 2013 - ACS Publications
Epihalohydrins [2-(halomethyl) oxiranes, 1, 2-epoxy-3-halopropanes](Figure 1) are well-
known versatile synthons and important reagents in the realm of organic synthesis …

Cooperative brønsted acid-type organocatalysis: alcoholysis of styrene oxides

T Weil, M Kotke, CM Kleiner, PR Schreiner - Organic Letters, 2008 - ACS Publications
We present a mild and efficient method for the completely regioselective alcoholysis of
styrene oxides utilizing a cooperative Brønsted acid-type organocatalytic system comprised …

Carbon dioxide fixation by cycloaddition with epoxides, catalyzed by biomimetic metalloporphyrins

D Bai, S Duan, L Hai, H **g - ChemCatChem, 2012 - Wiley Online Library
Several biomimetic metalloporphyrin complexes (M (TPP) XY; in which TPP= meso‐
porphyrin; M= MgII, AlIII, SnII, or SnIV; X= OAc, F, Cl, Br, I, OTf, or none; and Y= Cl, Br, I, OTf …

Nucleophilic ring-opening of epoxides: trends in β-substituted alcohols synthesis

M Fallah-Mehrjardi, AR Kiasat, K Niknam - Journal of the Iranian Chemical …, 2018 - Springer
The present review deals with the ring-opening of epoxides by various carbon, nitrogen,
oxygen, halogen, and sulfur-containing nucleophiles, which most of the resulting products …

Amberlyst-15 as a new and reusable catalyst for regioselective ring-opening reactions of epoxides to β-alkoxy alcohols

YH Liu, QS Liu, ZH Zhang - Journal of Molecular Catalysis A: Chemical, 2008 - Elsevier
Amberlyst-15 serves as an inexpensive, effective, and environmental friendly
heterogeneous catalyst for the regioselective ring-opening of epoxides by primary …

Graphite oxide: a simple and efficient solid acid catalyst for the ring-opening of epoxides by alcohols

M Mirza-Aghayan, M Alizadeh, MM Tavana… - Tetrahedron …, 2014 - Elsevier
A simple, efficient, and general procedure for the ring-opening of epoxides with various
alcohols to give the corresponding β-alkoxy alcohols using graphite oxide (GO) as the …

Regio-and stereoselective ring-opening reactions of epoxides with indoles and pyrroles in 2, 2, 2-trifluoroethanol.

M Westermaier, H Mayr - Chemistry (Weinheim an der Bergstrasse …, 2008 - europepmc.org
Aliphatic and aromatic epoxides react regio-and stereoselectively with indoles and pyrroles
in 2, 2, 2-trifluoroethanol without the use of a catalyst or any other additive. While aromatic …

Photoregulated fluorescence switching in axially coordinated tin (IV) porphyrinic dithienylethene

HJ Kim, JH Jang, H Choi, T Lee, J Ko, M Yoon… - Inorganic …, 2008 - ACS Publications
Photochromic fluorophore Sn (TTP)(DTE) 2, in which two phenolic derivatives of 1, 2-
dithienylethene are axially coordinated to (5, 10, 15, 20-tetratolylporphyrinato) tin (IV) in …