Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Lingaswamy, Kadari"'
Publikováno v:
New Journal of Chemistry
New Journal of Chemistry, Royal Society of Chemistry, 2020, 44 (37), pp.15928-15941. ⟨10.1039/D0NJ03470C⟩
New Journal of Chemistry, 2020, 44 (37), pp.15928-15941. ⟨10.1039/D0NJ03470C⟩
New Journal of Chemistry, Royal Society of Chemistry, 2020, 44 (37), pp.15928-15941. ⟨10.1039/D0NJ03470C⟩
New Journal of Chemistry, 2020, 44 (37), pp.15928-15941. ⟨10.1039/D0NJ03470C⟩
International audience; In this study, we developed a convenient methodology for the N-arylation of various acetamides, benzamides and related compounds by iodoferrocene. Optimization of the reaction was first performed from acetamide on the basis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17bb6018566532ff33e74728ce597bcc
https://doi.org/10.1039/d0nj03470c
https://doi.org/10.1039/d0nj03470c
Publikováno v:
Tetrahedron Letters. 60:1978-1981
Pd/Cu-catalyzed Heck type cross-coupling reaction of p-toluenesulfonylmethyl isocyanide (TosMIC) with various styrenes to access stilbenes in DMSO solvent under mild conditions is developed. This efficient and simple approach employs TosMIC as an ary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4da26bdd95c13b77d75c754e73955336
https://doi.org/10.1016/j.tetlet.2019.06.045
https://doi.org/10.1016/j.tetlet.2019.06.045
Autor:
William Erb, Palakodety Radha Krishna, Khadega Al-Mekhlafi, Florence Mongin, Vincent Dorcet, Thierry Roisnel, Lingaswamy Kadari
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2020, 362 (4), pp.832-850. ⟨10.1002/adsc.201901393⟩
Advanced Synthesis and Catalysis, 2020, 362 (4), pp.832-850. ⟨10.1002/adsc.201901393⟩
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2020, 362 (4), pp.832-850. ⟨10.1002/adsc.201901393⟩
Advanced Synthesis and Catalysis, 2020, 362 (4), pp.832-850. ⟨10.1002/adsc.201901393⟩
International audience; From 2-iodo-N,N-diisopropylferrocenecarboxamide, the halogen 'dance' reaction was applied to deliver gram quantities of the 3-iodo isomer. The latter was successfully functionalized by Ullmann-type and Suzuki-Miyaura cross-cou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b946854ae445a33ffa35501a5213d4ef
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02438541/document
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02438541/document
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2020, 52 (21), pp.3153-3161. ⟨10.1055/s-0040-1707175⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2020, 52 (21), pp.3153-3161. ⟨10.1055/s-0040-1707175⟩
SYNTHESIS, Georg Thieme Verlag, 2020, 52 (21), pp.3153-3161. ⟨10.1055/s-0040-1707175⟩
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2020, 52 (21), pp.3153-3161. ⟨10.1055/s-0040-1707175⟩
International audience; The 1,1′-disubstitution is currently the most frequent substitution pattern encountered in the ferrocene series. Here an original access based on the remote deprotometalation of N,N-diisopropyl-2-trimethylsilylferrocenecarbo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07c7574f12259c96b73a476da53d6751
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02948487
https://hal-univ-rennes1.archives-ouvertes.fr/hal-02948487
Publikováno v:
Organic Letters. 19:2580-2583
A novel iodine-catalyzed functionalization of a variety of olefins and alkynes and direct decarboxylative functionalization of cinnamic and propiolic acids with TosMIC to provide access to various vinyl, allyl, and β-iodo vinylsulfones is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beaefafe1199e04edbac1735a71f80c9
https://doi.org/10.1021/acs.orglett.7b00896
https://doi.org/10.1021/acs.orglett.7b00896
Autor:
Lingaswamy, Kadari1 (AUTHOR), Krishna, Palakodety Radha1 (AUTHOR), Prapurna, Y. Lakshmi1 (AUTHOR) ylprapurna.iict@gov.in
Publikováno v:
Synthetic Communications. 2016, Vol. 46 Issue 15, p1275-1282. 8p. 3 Diagrams, 2 Charts.
Publikováno v:
Advanced Synthesis & Catalysis. 358:3863-3868
A Mitsunobu approach for the synthesis of sulfinate esters by direct nucleophilic substitution of alcohols is described. The salient features of this strategy include neutral and metal-free conditions for the rapid synthesis of sulfinates in high yie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54f8fe4b9108745a8f19deb86d26c06a
https://doi.org/10.1002/adsc.201600997
https://doi.org/10.1002/adsc.201600997
Herein we report the stereoselective total synthesis of Exserolide F. The key step involves triflic acid catalyzed highly regioselective intramolecular cyclization of an O-alkynyl benzoic acid derivative to accomplish the core isocoumarin skeleton of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9a418217fdd622c125b3925a930986f
Akademický článek
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Publikováno v:
Synlett; 2016, Vol. 27 Issue 11, p1693-1698, 6p