Synthesis of quinolines, pyridine ligands and biological probes in green mediaThis work was presented at the Green Solvents for Catalysis Meeting, held in Bruchsal, Germany, 13–16th October 2002.

Bryson, Thomas A.; Gibson, James M.; Stewart, Jennifer J.; Voegtle, Heather L.; Tiwari, Abhishek; Dawson, John H.; Marley, W.; Harmon, B.

doi:10.1039/b211968d

Cited by 28 publications

(10 citation statements)

References 11 publications

(6 reference statements)

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“…The method presents a simple and useful synthetic process for quinaldines because of high yields, short reaction time, a straight forward, easy work-up procedure, the use of microwave A method for the synthesis of quinoline derivatives and bisquinoline derivatives (39) including a microwave-assisted, onepot-three-component reaction between aromatic amines, (36) aromatic aldehydes (37) and phenylacetylene (38) in the presence of catalytic amounts of potassium dodecatungstocobaltate trihydrate (K 5 CoW 12 O 40 $3H 2 O) has been demonstrated by Anvar and his co-workers (Scheme 2). 23 They were rst to report the use of polyoxometalates (POMs) as catalysts for the one-pot three-component synthesis of quinolines and bis-quinolines under microwave irradiation.…”

Section: Various Reaction Schemesmentioning

confidence: 99%

Recent advances in the synthesis of quinolines: a review

et al. 2014

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Section: Various Reaction Schemesmentioning

confidence: 99%

Recent advances in the synthesis of quinolines: a review

et al. 2014

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“…Substituted quinolines are frequently encountered in natural products (99), medicinal (100-108), and material chemistry (109)(110)(111)(112). The development of efficient method for their synthesis (113)(114)(115)(116)(117)(118)(119) or selective functionalization at different position is of immense importance (120)(121)(122)(123).…”

Section: Sp2 C-h Activationmentioning

confidence: 99%

Distant C-H Activation/Functionalization: A New Horizon of Selectivity Beyond Proximity

et al. 2015

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Activation/functionalization of inert C-H bond has undergone rapid growth in last decade and provides novel retro-synthetic disconnections for the synthesis of valuable molecules. The selectivity is often achieved by the use of directing group and is mainly limited to the proximal C-H bond. Initially, meta C-H activations were based on electronic or steric control and now it can be achieved by employing nitrile-based end-on-template as the directing group. The compilation of the remote C-H activation strategy will provide the useful linkage to the scientific community. This article is focused on recent progress in remote C-H activation, mechanistic understanding, and its applications in the field of total synthesis of targeted molecules.

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“…For example, o-aminocarbonyl compounds are unstable and not broadly commercially available. In an effort to overcome these limitations, Bryson et al have devised a method that allows for the in situ preparation of o-aminobenzaldehydes by reduction of the corresponding o-nitrobenzaldeydes [343].…”

Section: Pyridines and Quinolinesmentioning

confidence: 99%