Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Kande K. D. Amarasinghe"'
Autor:
Kande K. D. Amarasinghe, Sanjoy K. Chowdhury, Jeongbeob Seo, John Montgomery, Alexey V. Savchenko, Eric Oblinger
Publikováno v:
Pure and Applied Chemistry. 74:129-133
Substrates that possess an a,b-unsaturated carbonyl tethered to an alkyne have been utilized in a variety of nickel-catalyzed processes. Depending on ligand structure, reagent structure, reaction conditions, and workup conditions, several different m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::850ce41087421f381ac23fba2e399e23
https://doi.org/10.1351/pac200274010129
https://doi.org/10.1351/pac200274010129
Publikováno v:
Organic Letters. 4:1743-1745
[reaction: see text] 1,3-Dienes were prepared by a variety of nickel-catalyzed couplings and cyclization processes. Intermolecular or partially intramolecular couplings of alkynes, vinylzirconium reagents, and either aldehydes or enones efficiently p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ab340df0c36f532d1375830136354e4
https://doi.org/10.1021/ol025812+
https://doi.org/10.1021/ol025812+
Publikováno v:
Organometallics. 20:370-372
Two metallacycles derived from the oxidative cyclization of nickel(0) with an alkynyl enal have been isolated and fully characterized. The metallacycles obtained possess an η1 nickel O-enolate motif within the metallacyclic framework.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe73328430f83ef9204e68d2e0d9409a
https://doi.org/10.1021/om0010013
https://doi.org/10.1021/om0010013
Publikováno v:
ChemInform. 33
1,3-Dienes were prepared by a variety of nickel-catalyzed couplings and cyclization processes. Intermolecular or partially intramolecular couplings of alkynes, vinylzirconium reagents, and either aldehydes or enones efficiently proceeded to generate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94f7051db0027f0e871fdfcc84be34d1
https://doi.org/10.1002/chin.200240065
https://doi.org/10.1002/chin.200240065
Autor:
Kande K. D. Amarasinghe, Alexey V. Savchenko, Sanjoy K. Chowdhury, Jeongbeob Seo, John Montgomery, Eric Oblinger
Publikováno v:
ChemInform. 33
Substrates that possess an α,β-unsaturated carbonyl tethered to an alkyne have been utilized in a variety of nickel-catalyzed processes. Depending on ligand structure, reagent structure, reaction conditions, and workup conditions, several different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b69520c5e21e8bbb2e1f3cbe2fd7cd1
https://doi.org/10.1002/chin.200248253
https://doi.org/10.1002/chin.200248253
Publikováno v:
ChemInform. 33
An enantioselective total synthesis of (+)-testudinariol A was completed. A new nickel-catalyzed allenyl aldehyde cyclization was developed in the approach. In addition, an asymmetric anti aldol reaction and a two-directional oxocarbenium ion/vinyl s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7ff8af4256029a3125f2fd5c558cb7f
https://doi.org/10.1002/chin.200251181
https://doi.org/10.1002/chin.200251181
Autor:
Kande K. D. Amarasinghe, et al. et al.
Publikováno v:
ChemInform. 37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e6ad101f080cf50142751529e5f387f
https://doi.org/10.1002/chin.200651111
https://doi.org/10.1002/chin.200651111
Autor:
Kande K D, Amarasinghe, Artem G, Evdokimov, Artem G, Evidokimov, Kevin, Xu, Cynthia M, Clark, Matthew B, Maier, Anil, Srivastava, Anny-Odile, Colson, Gina S, Gerwe, George E, Stake, Brian W, Howard, Matthew E, Pokross, Jeffrey L, Gray, Kevin G, Peters
Publikováno v:
Bioorganicmedicinal chemistry letters. 16(16)
The sulfamic acid phosphotyrosine mimetic was coupled with a previously known malonate template to obtain highly selective and potent inhibitors of HPTPbeta. Potentially hydrolyzable malonate ester functionalities were replaced with 1,2,4-oxadiazoles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba3c05f79a1a4e620626ea01c44e4375
https://pubmed.ncbi.nlm.nih.gov/16759857
https://pubmed.ncbi.nlm.nih.gov/16759857
Autor:
Andy R. L. Skauge, Mary Jane Heeg, Gireesh M. Mahandru, Kande K. D. Amarasinghe, Sanjoy K. Chowdhury, John Montgomery
Publikováno v:
Journal of the American Chemical Society. 125(44)
A new strategy for effecting cascade cyclization processes using nickel enolates has been developed. Nickel enolates may be cleanly generated by the oxidative cyclization of an enal and alkyne with Ni(0), and the resulting enolate may be functionaliz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44ff77c755dcf2bd4039f9d5650e4dc3
https://pubmed.ncbi.nlm.nih.gov/14583044
https://pubmed.ncbi.nlm.nih.gov/14583044
Publikováno v:
Organic letters. 5(20)
[structure: see text] The first total synthesis and stereochemical definition of isodomoic acid G has been achieved. The key nickel-catalyzed coupling of an alkynyl enone with an alkenylzirconium allows formation of the pyrrolidine ring and most of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27e6d02e167dad866e2585b47993a2db
https://pubmed.ncbi.nlm.nih.gov/14507227
https://pubmed.ncbi.nlm.nih.gov/14507227