In 2007 the members of the ACS Green Chemistry Institute® Pharmaceutical Roundtable
assembled a list of key green chemistry research areas to both identify transformations that …

The direct, catalytic dehydrative substitution of alcohols is a challenging, yet highly desirable
process in the development of more sustainable approaches to organic chemistry. This …

Nucleophilic substitution reactions of alcohols are among the most fundamental and
strategically important transformations in organic chemistry. For over half a century, these …

Nucleophilic substitutions (SN) account for the most essential and frequently applied
chemical transformations. SN‐reactions allow forging C–C, C–O, C–N and C–Cl bonds, for …

Optically pure alcohols are abundant in nature and attractive as feedstock for organic
synthesis but challenging for further transformation using atom efficient and sustainable …

Benzofuran and naphthofuran derivatives are synthesized from readily available phenols
and naphthols. Regioselective ring openings of 2 H-azirine followed by in situ aromatization …

Chemical bonding properties are crucial to understanding the chemical behavior of
molecules. Spectroscopy is a versatile technical tool to study various microscopic properties …

Abstract A Deep Eutectic Solvent, choline chloride/glycerol (1: 2 mol mol− 1), proved to be
an effective and sustainable reaction medium to promote telescoped, one‐pot Mizoroki …

The catalytic deoxyamination of readily available 2‐arylethanols offers an appealing, simple,
and straightforward means of accessing β‐(hetero) arylethylamines of biological interest …

Direct substitution of alcohols has been a popular topic in organic chemistry.
Deoxyhalogenation of alcohols represents one of the most important transformations for …