Highly functionalized organomagnesium reagents prepared through halogen–metal exchange

P Knochel, W Dohle, N Gommermann… - Angewandte Chemie …, 2003 - Wiley Online Library
Organomagnesium reagents occupy a central position in synthetic organic and
organometallic chemistry. Recently, the halogen–magnesium exchange has considerably …

Synthese hoch funktionalisierter Organomagnesiumreagentien durch Halogen‐Metall‐Austausch

P Knochel, W Dohle, N Gommermann… - Angewandte …, 2003 - Wiley Online Library
Magnesiumverbindungen spielen eine zentrale Rolle in der präparativen organischen und
metallorganischen Chemie. Seit kurzem ermöglicht der Halogen‐Magnesium‐Austausch …

Selective Halogen− Magnesium exchange reaction via organomagnesium ate complex

A Inoue, K Kitagawa, H Shinokubo… - The Journal of Organic …, 2001 - ACS Publications
Halogen− magnesium exchange of various aryl halides is achieved with a magnesium ate
complex at low temperatures. Tributylmagnesate (n Bu3MgLi) induces facile iodine …

Halogen bonding and mechanochemistry combined: synthesis, characterization, and application of N-iodosaccharin pyridine complexes

C Schumacher, KN Truong, JS Ward… - Organic Chemistry …, 2024 - pubs.rsc.org
Halogen-bonded complexes are utilized across a myriad of synthetic chemistry fields, with
halogen (I) complexes such as Barluenga's reagent being ubiquitous in halogenation …

Functionalized magnesium organometallics as versatile intermediates for the synthesis of polyfunctional heterocycles

H Ila, O Baron, AJ Wagner, P Knochel - Chemical communications, 2006 - pubs.rsc.org
In the last few years, we have demonstrated that the halogen/magnesium-exchange reaction
is a unique method for preparing a variety of new functionalized aryl, alkenyl, heteroaryl …

Copper/Persulfate‐Promoted Oxidative Decarboxylative C− H Acylation of Pyrazolones with α‐Oxocarboxylic Acids: Direct Access to 4‐Acylpyrazolones under Mild …

T Kittikool, A Thupyai, K Phomphrai… - Advanced Synthesis & …, 2018 - Wiley Online Library
A facile and efficient oxidative C− H acylation of N‐substituted pyrazolones using α‐
oxocarboxylic acids as an acyl group source was developed. A combination of Cu (OAc) 2 …

New methods of imidazole functionalization-from imidazole to marine alkaloids

H Du, Y He, R Sivappa, CJ Lovely - Synlett, 2006 - thieme-connect.com
The pyrrole-imidazole family of marine alkaloids, the so-called oroidin natural products,
exhibits an impressive diversity of structural motifs. The majority of these natural products …

Copper-catalyzed acylation of pyrazolones with aldehydes to afford 4-acylpyrazolones

Y Xiao, X Wu, J Teng, S Sun, JT Yu… - Organic & biomolecular …, 2019 - pubs.rsc.org
Copper-catalyzed direct acylation of the alkenyl C–H bond in 1, 2-dihydro-3H-pyrazol-3-
ones has been developed, affording a series of 4-acylpyrazolones in moderate to good …

Concise total synthesis of naamine G and naamidine H

PB Koswatta, CJ Lovely - Chemical communications, 2010 - pubs.rsc.org
Concise total synthesis of naamine G and naamidine H - Chemical Communications (RSC
Publishing) DOI:10.1039/B926285G Royal Society of Chemistry ViewáPDFáVersionPreviousáArticleNextáArticle …

Total synthesis and cytotoxicity of Leucetta alkaloids

PB Koswatta, S Kasiri, JK Das, A Bhan, HM Lima… - Bioorganic & medicinal …, 2017 - Elsevier
The total synthesis of a number of representative natural products isolated from Leucetta
and Clathrina sponges containing a polysubstituted 2-aminoimidazole are described. These …