Catalytic functionalization of indoles in a new dimension

M Bandini, A Eichholzer - Angewandte Chemie International …, 2009 - Wiley Online Library
Abstract 140 Years ago Adolf von Baeyer proposed the structure of a heteroaromatic
compound which revolutionized organic and medical chemistry: indole. After more than a …

[HTML][HTML] A review of new developments in the Friedel–Crafts alkylation–From green chemistry to asymmetric catalysis

M Rue**, BJ Nachtsheim - Beilstein Journal of Organic …, 2010 - beilstein-journals.org
The development of efficient Friedel–Crafts alkylations of arenes and heteroarenes using
only catalytic amounts of a Lewis acid has gained much attention over the last decade. The …

Base-Catalyzed Aryl-B(OH)2 Protodeboronation Revisited: From Concerted Proton Transfer to Liberation of a Transient Aryl Anion

PA Cox, M Reid, AG Leach, AD Campbell… - Journal of the …, 2017 - ACS Publications
Pioneering studies by Kuivila, published more than 50 years ago, suggested ipso
protonation of the boronate as the mechanism for base-catalyzed protodeboronation of …

Key green chemistry research areas—a perspective from pharmaceutical manufacturers

DJC Constable, PJ Dunn, JD Hayler, GR Humphrey… - Green …, 2007 - pubs.rsc.org
In 2005, the ACS Green Chemistry Institute (GCI) and the global pharmaceutical
corporations developed the ACS GCI Pharmaceutical Roundtable to encourage the …

Recent approaches for C–C bond formation via direct dehydrative coupling strategies

R Kumar, EV Van der Eycken - Chemical Society Reviews, 2013 - pubs.rsc.org
In recent years, reaction of inexpensive and abundantly available alcohols (C–OH) with
unactivated nucleophilic coupling partners (C–H), leading to the construction of the C–C …

Direct Nucleophilic SN1‐Type Reactions of Alcohols

E Emer, R Sinisi, MG Capdevila… - European Journal of …, 2011 - Wiley Online Library
Abstract In 2005, the ACS Green Chemistry Institute (GCI) and the global pharmaceutical
corporations developed the ACS GCI Pharmaceutical Roundtable to encourage the …

Organocatalytic Asymmetric Alkylation of Aldehydes by SN1‐Type Reaction of Alcohols

PG Cozzi, F Benfatti, L Zoli - Angewandte Chemie International …, 2009 - Wiley Online Library
Organocatalytic Asymmetric Alkylation of Aldehydes by SN1‐Type Reaction of Alcohols -
Cozzi - 2009 - Angewandte Chemie International Edition - Wiley Online Library Skip to Article …

Surfactant-type Brønsted acid catalyzed dehydrative nucleophilic substitutions of alcohols in water

S Shirakawa, S Kobayashi - Organic Letters, 2007 - ACS Publications
A protocol for the dehydrative nucleophilic substitution of benzyl alcohols with a variety of
carbon-and heteroatom-centered nucleophiles using dodecylbenzenesulfonic acid (DBSA) …

Nucleophilic substitution reactions of alcohols with use of montmorillonite catalysts as solid Brønsted acids

K Motokura, N Nakagiri, T Mizugaki… - The Journal of …, 2007 - ACS Publications
We have developed an environmentally benign synthetic approach to nucleophilic
substitution reactions of alcohols that minimizes or eliminates the formation of byproducts …

Brønsted acid catalyzed propargylation of 1, 3-dicarbonyl derivatives. Synthesis of tetrasubstituted furans

R Sanz, D Miguel, A Martínez… - Organic …, 2007 - ACS Publications
Simple Brønsted acids such as p-toluenesulfonic acid monohydrate (PTS) efficiently
catalyze a direct substitution of the hydroxyl group in propargylic alcohols with 1, 3 …