Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Ragam Raju"'
1
Metal- and base-free syntheses of aryl/alkylthioindoles by the iodine-induced reductive coupling of aryl/alkyl sulfonyl chlorides with indoles
Autor: Ragam Raju, Vykunthapu Narayanarao, Gullapalli Kumaraswamy
Publikováno v: RSC Advances. 5:22718-22723
An Iodine-catalysed process for an efficient and scalable sulfenylation protocol for indoles employing aryl-/alkyl sulfonyl chlorides has been developed. A series of sterically and electronically divergent aryl-/alkyl sulfonyl chlorides participated
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::73bd2a671d21d5fa9181ffff5f0400a4
https://doi.org/10.1039/c5ra00646e
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2
Concise diastereoselective synthesis of calcaripeptide C via asymmetric transfer hydrogenation/Pd-induced chiral allenylzinc as a key reaction
Autor: Vykunthapu Narayanarao, Gullapalli Kumaraswamy, Ragam Raju
Publikováno v: Organic & Biomolecular Chemistry. 13:8487-8494
Synthesis of the natural product calcaripeptide C derived from the fungal metabolite mycelium KF525 of Calcarisporium sp. has been achieved. This complementary approach avoids the use of a stoichiometric amount of chiral auxiliary reagents as commonl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d6524662b7d8e763abac8493b12119e
https://doi.org/10.1039/c5ob01164g
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4
An expedient synthesis of enantioenriched substituted (2-benzofuryl)arylcarbinols via tandem Rap–Stoermer and asymmetric transfer hydrogenation reactions
Autor: Ragam Raju, Gullapalli Kumaraswamy, Mogilisetti Padmaja, Gajula Ramakrishna
Publikováno v: Tetrahedron. 66:9814-9818
An expedient synthesis of enantioenriched substituted (benzofuran-yl)-aryl and heteroaryl carbinols, is described. A key feature of this protocol is synthesis of functionally varied benzofuran scaffolds via a Rap–Stoermer reaction/catalytic asymmet
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fb83a1722a0d771567668e59323fee6d
https://doi.org/10.1016/j.tet.2010.10.074
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6
ChemInform Abstract: Metal- and Base-Free Syntheses of Aryl/Alkylthioindoles by the Iodine-Induced Reductive Coupling of Aryl/Alkyl Sulfonyl Chlorides with Indoles
Autor: Vykunthapu Narayanarao, Gullapalli Kumaraswamy, Ragam Raju
Publikováno v: ChemInform. 46
An Iodine-catalysed process for an efficient and scalable sulfenylation protocol for indoles employing aryl-/alkyl sulfonyl chlorides has been developed. A series of sterically and electronically divergent aryl-/alkyl sulfonyl chlorides participated
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d381d78a5ecdfa01d0b6de27ba48b727
https://doi.org/10.1002/chin.201530167
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8
ChemInform Abstract: An Expedient Synthesis of Enantioenriched Substituted (2-Benzofuryl) Arylcarbinols via Tandem Rap-Stoermer and Asymmetric Transfer Hydrogenation Reactions
Autor: Ragam Raju, Gullapalli Kumaraswamy, Gajula Ramakrishna, Mogilisetti Padmaja
Publikováno v: ChemInform. 42
An expedient synthesis of enantioenriched substituted (benzofuran-yl)-aryl and heteroaryl carbinols, is described. A key feature of this protocol is synthesis of functionally varied benzofuran scaffolds via a Rap–Stoermer reaction/catalytic asymmet
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::90ff75ef03cd29daa5f50d3acc18e87d
https://doi.org/10.1002/chin.201118091
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