Zobrazeno 1 - 10
of 12
pro vyhledávání: '"T D Suja"'
Autor:
Rajeev S. Menon, T. D. Suja
Publikováno v:
Copper Catalysis in Organic Synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01792563f2a2ea73d5b0737d5efff67f
https://doi.org/10.1002/9783527826445.ch10
https://doi.org/10.1002/9783527826445.ch10
Publikováno v:
Synthesis. 48:4207-4212
A one-pot synthesis of highly substituted pyrazoles that are fused to dihydrochromenes, dihydroquinolines and cyclopentane motifs, from readily available precursors is reported. The reaction involves conversion of alkyne-tethered aldehydes into the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af4d270b6cee5f241f5cbc253d96ca87
https://doi.org/10.1055/s-0035-1562533
https://doi.org/10.1055/s-0035-1562533
Publikováno v:
ChemInform. 47
A series of aminonaphthoquinone—sulfonylamidine conjugates of type (IV) or (VII) are prepared.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d04870ab29e0b4a7cfd2ca9598b78f8
https://doi.org/10.1002/chin.201632076
https://doi.org/10.1002/chin.201632076
Autor:
G Vijay Nair, T. D. Suja
Publikováno v:
Tetrahedron. 63:12247-12275
A detailed discussion on the application of [3+2] dipolar cycloaddition reactions in targeted syntheses is presented. Figure options Download full-size image Download as PowerPoint slide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0daea4f8da5d850e68ba72293b497547
https://doi.org/10.1016/j.tet.2007.09.065
https://doi.org/10.1016/j.tet.2007.09.065
Publikováno v:
Bioorganicmedicinal chemistry letters. 26(8)
A series of aminonaphthoquinone-sulfonylamidine conjugates were synthesized via a copper-catalyzed three-component reaction of N-propargyl aminonaphthoquinone, sulfonyl azides and various amines. Majority of the compounds exhibited promising antiprol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a0d16f35eb0423883928f0da304c5a3
https://pubmed.ncbi.nlm.nih.gov/26948541
https://pubmed.ncbi.nlm.nih.gov/26948541
Publikováno v:
Synthesis. 2006:2335-2338
1,3-Dicarbonyl compounds react with methylenecyclopropanes by oxidation with CAN to give spirocyclopropyl dihydro-furan derivatives in good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b427e521674b4ccb5a8055ec300bb35
https://doi.org/10.1055/s-2006-942371
https://doi.org/10.1055/s-2006-942371
Publikováno v:
Tetrahedron Letters. 47:705-709
The stereoselective intramolecular cyclization of epoxypropyl cinnamyl amines mediated by substoichiometric quantities of CAN leading to the synthesis of functionalized piperidines and the formation of a supramolecular assembly of the latter with eth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67b8656d35e1a0894ac49c5e295672d6
https://doi.org/10.1016/j.tetlet.2005.11.115
https://doi.org/10.1016/j.tetlet.2005.11.115
Autor:
G Vijay Nair, T. D. Suja
Publikováno v:
ChemInform. 39
A detailed discussion on the application of [3+2] dipolar cycloaddition reactions in targeted syntheses is presented. Figure options Download full-size image Download as PowerPoint slide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00b0d4dc62e2eb6fb875aeb0a52835cf
https://doi.org/10.1002/chin.200811234
https://doi.org/10.1002/chin.200811234
Publikováno v:
ChemInform. 37
Oxidative ring expansion of methylenecyclopropanes with CAN under oxygen atmosphere was investigated. A facile conversion affording 2,2-diarylcyclobutanones occurred in good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::213fc2d80fd74677060dce96d45459bf
https://doi.org/10.1002/chin.200649094
https://doi.org/10.1002/chin.200649094
Publikováno v:
ChemInform. 37
The stereoselective intramolecular cyclizations of bis(cinnamyl)tosylamides and dimethyl bis(cinnamyl)malonates mediated by cerium(IV) ammonium nitrate leading to the synthesis of 3,4-trans-disubstituted pyrrolidines and cyclopentanes are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d6d59f8804a2c10e47d8a6a179b7723
https://doi.org/10.1002/chin.200630117
https://doi.org/10.1002/chin.200630117