Mother Nature needs to be protected from ever increasing chemical pollutions associated
with synthetic organic processes. The fundamental challenge for today's methodologists is to …

Selective protection of− NH2 functionality has enormous utility and significance in organic
synthesis. Amines are nucleophile and basic in nature thus vulnerable to react with an …

We report a mild method for the selective deprotection of the N-Boc group from a structurally
diverse set of compounds, encompassing aliphatic, aromatic, and heterocyclic substrates by …

In this paper a new catalyst-free and on-water method for protection of amines and amino
acids with di-tert-butyl dicarbonate, 9-fluorenylmethoxycarbonyl chloride, acetyl chloride and …

Macrocycles based on directional bonding and dynamic covalent bond exchange can be
designed with specific pore shapes, sizes, and functionality. These systems retain many of …

A new series of 2‐aminobenzothiazole derivatives was designed, synthesized and
evaluated for their anticancer activity against the MCF7, MDAMB‐231, and HepG2 cancer …

An efficient and convenient one-pot synthesis of novel α-sulfamidophosphonates is
described via a three-component reaction. This reaction was carried out through a three …

Recently, benzothiazole derivatives have garnered significant attention among the research
community due to their pharmaceutical and biological significance. Likewise, in this study …

A new environmentally benign, simple, and efficient protocol for the chemoselective
sulfonylation of various structural amines using microwave irradiation under solvent-and …

2-[18 F] Fluorophenylalanine (2-[18 F] FPhe), a promising PET tracer for imaging of cerebral
infarction and tumors, was efficiently prepared from an easily accessible iodonium salt …