Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Ponminor Senthil Kumar"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 3, Iss 1, p 49 (2007)
An intramolecular Schmidt reaction strategy for the synthesis of various derivatives of crispine A using azido-ketone as a key intermediate is described.
Externí odkaz:
https://doaj.org/article/3ef85dbcd63b4bb4adbed084fdbf36f3
Autor:
Sundarababu Baskaran, Marc Lamshöft, Manohar Puppala, Kenneth O. Eyong, Gabriel N. Folefoc, Michael Spiteller, Ponminor Senthil Kumar
Publikováno v:
Org. Biomol. Chem.. 11:459-468
The Hooker oxidation is one of the most intriguing transformations wherein lapachol (1) is readily converted to norlapachol (2) in very good yield. This one-pot reaction involves a very intricate mechanism in which the alkyl side chain of lapachol is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77c19a245318be1150dca105b644efab
https://doi.org/10.1039/c2ob26737c
https://doi.org/10.1039/c2ob26737c
Publikováno v:
European Journal of Organic Chemistry. 2011:6980-6988
A diversity-oriented synthesis is described for functionalized chiral building blocks (i.e., 7, 9, 10, 16, and 17) and the biologically active iminosugar, fucosidase inhibitor (2S,3R,4R,5R)-2-(hydroxymethyl)-5- methylpyrrolidine-3,4-diol (22), starti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a944e18c53f40122c31ecbb17ad7db2c
https://doi.org/10.1002/ejoc.201100968
https://doi.org/10.1002/ejoc.201100968
Publikováno v:
Angewandte Chemie. 122:816-819
(Chemical Equation Presented) Ruthenium has twice the fun: The synthetic potential of the highly regio- and stereoselective title reaction, which relies on two oxidative cleavage steps promoted by RuCI3 in combination with NaIO 4 (see example; Bz = b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c7aae97a52414b8d6527ea16128b2d5
https://doi.org/10.1002/ange.200905952
https://doi.org/10.1002/ange.200905952
Publikováno v:
Tetrahedron Letters. 50:3489-3492
A stereoselective synthesis of N-Boc-protected cis-(2R,3S)-3-hydroxy pipecolic acid, starting from d-glucose is described. The key step in the overall synthesis is a highly regioselective reductive cleavage of benzylidene acetal 13 leading to hydroxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13859fafe445c67c2d8b1a634bf133af
https://doi.org/10.1016/j.tetlet.2009.03.007
https://doi.org/10.1016/j.tetlet.2009.03.007
Publikováno v:
European Journal of Organic Chemistry. 2008:6063-6067
Phosphomolybdic acid supported on silica gel provides a truly catalytic method for the chemoselective cleavage of benzylidene acetals having sensitive functional groups under mild conditions. It is easy to perform on large scale owing to minimal cata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bb50c4bca2827dae285240e50864bd4
https://doi.org/10.1002/ejoc.200800963
https://doi.org/10.1002/ejoc.200800963
Publikováno v:
IndraStra Global.
A mild and highly efficient one-pot method has been developed for the stereoselective synthesis of structurally diverse novel iminosugar C-aryl glycosides. The generality of this methodology is demonstrated with a wide variety of aryl nucleophiles an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6ccdeb7dce4a164a3115c4cb5d77d43
http://hdl.handle.net/11717/15457
http://hdl.handle.net/11717/15457
Publikováno v:
ChemInform. 43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96bbee4987b6d7680f8372fe08659ee6
https://doi.org/10.1002/chin.201214030
https://doi.org/10.1002/chin.201214030
Publikováno v:
ChemInform. 41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0f405fdac976717bbf6a007c3cea0d5
https://doi.org/10.1002/chin.201021035
https://doi.org/10.1002/chin.201021035
Publikováno v:
ChemInform. 40
Phosphomolybdic acid supported on silica gel provides a truly catalytic method for the chemoselective cleavage of benzylidene acetals having sensitive functional groups under mild conditions. It is easy to perform on large scale owing to minimal cata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::567c826425d7ab8d0a71b6f83b173f28
https://doi.org/10.1002/chin.200919048
https://doi.org/10.1002/chin.200919048