The present review “Iron Catalysis in Organic Synthesis” covers the literature until the end of
June 2014 and represents a comprehensive update of a previous article published by Bolm …

According to the CRC dictionary of natural products, 1 90% of chemically individual
molecules discovered in nature contain either a carbocyclic or a heterocyclic subunit. 2 Not …

The Prins reaction 1 is often related to the Kriewitz reaction. 2 The latter leads to unsaturated
alcohol 1 from a-pinene and formaldehyde through a thermal 'ene-rearrangement'(Eq. 1) …

A simple, straightforward, and highly efficient diastereoselective multicomponent one-pot
synthesis of a series of pharmaceutically interesting functionalized piperidine derivatives …

Tetrabutylammonium tribromide (TBATB) has been found to be an efficient catalyst for the
one-pot synthesis of highly substituted piperidines through a combination of 1, 3-dicarbonyl …

A simple and convenient one-pot multicomponent reaction (MCR) has been developed for
the synthesis of highly functionalized piperidines catalyzed by molecular iodine. This …

A new Prins cyclization process that builds up one carbon− carbon bond, one heteroatom-
carbon bond, and one halogen-carbon bond,(in an oxa-and azacycle) relies on an iron …

The first total syntheses of aflavazole (6) and 14-hydroxyaflavinine (8), two sterically
congested indole diterpenoids, were accomplished. AlI3-promoted alkyne Prins cyclization …

In this report, we describe a halo-Prins/aryl halo-Nazarov cyclization strategy that employs
readily available starting materials, inexpensive reagents, and convenient reaction …

Iron-Catalyzed Redox Radical Cyclizations of 1,6-Dienes and Enynes | Organic Letters ACS
ACS Publications C&EN CAS Find my institution Log In Organic Letters ACS Publications …