Iron catalysis in organic synthesis

I Bauer, HJ Knölker - Chemical reviews, 2015 - ACS Publications
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 …

Use of bromine and bromo-organic compounds in organic synthesis

I Saikia, AJ Borah, P Phukan - Chemical reviews, 2016 - ACS Publications
Bromination is one of the most important transformations in organic synthesis and can be
carried out using bromine and many other bromo compounds. Use of molecular bromine in …

Recent developments in asymmetric aziridination

H Pellissier - Tetrahedron, 2010 - Elsevier
Aziridines are saturated three-membered heterocycles containing one nitrogen atom. These
compounds are among the most fascinating intermediates in organic synthesis, acting as …

Application of N-halo reagents in organic synthesis

E Kolvari, A Ghorbani-Choghamarani, P Salehi… - Journal of the Iranian …, 2007 - Springer
This review article summarizes published data on the application of N-halo reagents (such
as N-halo amines, N-halo amides and/or imides, N-halo sulfonamides and/or imides, and …

Non-heme iron catalysts for epoxidation and aziridination reactions of challenging terminal alkenes: towards sustainability

A Fingerhut, OV Serdyuk, SB Tsogoeva - Green Chemistry, 2015 - pubs.rsc.org
Through catalytic epoxidation and aziridination of olefins versatile synthetic intermediates
and subunits of biologically active compounds and pharmaceuticals–epoxides and …

Copper-Catalyzed Alkene Aziridination with N-Tosyloxycarbamates

H Lebel, S Lectard, M Parmentier - Organic Letters, 2007 - ACS Publications
Pyridine copper complexes were found as active catalysts for the intramolecular
aziridination of allylic N-tosyloxycarbamates and the intermolecular aziridination of styrenes …

Comparative nitrene-transfer chemistry to olefinic substrates mediated by a library of anionic Mn (II) triphenylamido-amine reagents and M (II) congeners (M= Fe, Co …

V Bagchi, A Kalra, P Das, P Paraskevopoulou… - ACS …, 2018 - ACS Publications
Selective amination of σ and π entities such as C–H and C═ C bonds of substrates remains
a challenging endeavor for current catalytic methodologies devoted to the synthesis of …

Cationic Divalent Metal Sites (M= Mn, Fe, Co) Operating as Both Nitrene-Transfer Agents and Lewis Acids toward Mediating the Synthesis of Three-and Five …

SK Sahoo, B Harfmann, L Ai, Q Wang… - Inorganic …, 2023 - ACS Publications
The tripodal compounds [(TMG3trphen) MII–solv](PF6) 2 (M= Mn, Fe, Co; solv= MeCN, DMF)
and bipodal analogues [(TMG2biphen) MII (NCMe) x](PF6) 2 (x= 3 for Mn, Fe; x= 2 for Co) …

Recent progress in the application of N-halo reagents in the synthesis of heterocyclic compounds

H Veisi, R Ghorbani-Vaghei - Tetrahedron, 2010 - Elsevier
Of the more than 20 million chemical compounds currently registered, about one half contain
heterocyclic systems. Heterocycles are important, not only because of their abundance, but …

The (Porphyrin) ruthenium‐Catalyzed Aziridination of Olefins Using Aryl Azides as Nitrogen Sources

S Fantauzzi, E Gallo, A Caselli, C Piangiolino… - 2007 - Wiley Online Library
Aryl azides have been used as atom‐efficient nitrene transfer reagents in the (porphyrin)
ruthenium‐catalyzed amination of olefins. Several azides, olefins and [Ru (porphyrin) CO] …