Quinoline is one of the most important nitrogen containing heterocycles, being widespread
in nature and present in a broad variety of pharmacologically active compounds …

Chemoselectivity is an important issue frequently encountered while working over labile
precursors. Carbonyl compounds with a heteroatom at the β carbon are sensitive precursors …

Despite being a very useful C–C bond forming and highly applicative reaction, Morita–Baylis–
Hillman (MBH) reaction has been limited by its excessive slow reaction rate, including its …

The Na2S-mediated facile synthesis of terminal alkynes from gem-dibromoalkenes, at
20/40° C under open flask conditions has been developed. Various precursors derived from …

Use of acrylamide as an activated alkene in largely recognized Morita Baylis Hillman (MBH)
reaction has been least explored owing to less reactivity of acrylamide as Michael acceptor …

Simple, environmentally benign and metal free one pot strategy has been used for the
synthesis of 4-iodo-3-phenylbenzo [b][1, 6] naphthyridine from O-alkynylquinolinyl …

An efficient synthetic route to highly functionalized naphthalenes and quinolines has been
developed using domino reactions between Morita–Baylis–Hillman (MBH) acetates and …

An efficient synthetic route to highly substituted dihydroquinolines and
dihydronaphthyridines has been developed using a domino reaction of Morita-Baylis …

A simple, highly efficient, and regioselective synthesis of functionalized phenanthridines by
the reaction of MBH acetates of 2‐chloroquinoline‐3‐carbaldehydes with nitroalkanes is …

Simple, Metal free, eco-friendly one pot strategy for the synthesis of 4-iodo-3-phenylbenzo
[b][1, 6] naphthyridine is described from O-alkynylquinolinyl aldehydes with tert butyl amine …