The direct α‐Csp2 H functionalization and thiomethylation of α‐oxoketene dithioacetals
(DTAs) has been accomplished with dimethyl sulfoxide (DMSO) in the presence of iodine …

Abstract β-Allyl-β-hydroxy dithioesters have been employed in the synthesis of hitherto
unreported and synthetically demanding 2 H-thiopyrans via regioselective intramolecular …

Synthesis of thiophene derivatives through InCl3-catalyzed cyclization of β-oxodithioesters with
vinyl azides - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books …

An organic molecule which behaves like a superalkali has been designed from an aromatic
heterocyclic molecule, pyrrole. Using first-principles calculation and a systematic two-step …

Aromatic heterocyclic molecules play an important role in synthetic organic chemistry due to
their wide range of reactivities. Because of their aromaticity, they have a lower tendency to …

Two ferrocene derivatives with appended pyrazole substituents, namely, 1, 1′-bis (5-methyl-
1 H-pyrazol-3-yl) ferrocene (H2LH) and 1, 1′-bis (5-trifluoromethyl-1 H-pyrazol-3-yl) …

An efficient and highly regioselective one‐pot three‐component synthesis of previously
inaccessible and synthetically demanding 3‐(cycloalkyl/alkyl/arylamino)‐5 …

DMAP mediated one-pot domino thienannulation: a versatile, regioselective and green
mechanochemical route to naphtho[2,3- b ]thiophenes - RSC Advances (RSC Publishing) …

Indium triflate mediated first synthesis of diversely functionalized pyrrol-2-thiones has been
developed by dehydrative annulation of β-ketothioamides with phenylglyoxal through the …

A versatile and convenient one-pot direct approach to 2, 3-disubstituted benzo/naphtho [b]
furans via domino annulation of α-oxoketene dithioacetals and 1, 4-benzo/naphthoquinone …