Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Jessica Salvadori"'
Publikováno v:
Synlett. 2011:199-202
Hydroformylation is a powerful reaction that has suffered for some negative prejudices related to the use of gaseous H 2 and CO. Now it is possible to carry out hydroformylation and different cyclohydrocarbonylations, even on complex substrates, usin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3a2a64c3753deff6687fc30a46009b9
https://doi.org/10.1055/s-0030-1259281
https://doi.org/10.1055/s-0030-1259281
Autor:
Nicolas Girard, Etienne Airiau, Maurizio Taddei, Jessica Salvadori, Giacomo Lonzi, Elena Petricci, Claire Chemin, André Mann
Publikováno v:
Synthesis. 2010:2901-2914
Hydroformylation of alkenes can be carried out in short time and with low syngas pressure under microwave (MW) dielectric heating. Alkenes, carrying O-, N-, or C-nucleophilic fragments, can be designed for domino reactions, mainly cyclocondensations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30a4367cc39966a1ebcf71bc7d100e38
https://doi.org/10.1055/s-0030-1258207
https://doi.org/10.1055/s-0030-1258207
Publikováno v:
Tetrahedron. 66:3749-3753
A multicomponent reaction that employs an unsaturated carboxylic acid, a 1,2 or 1,3 amino alcohol and gaseous CO and H2 has been discovered. Thus, hydrocarbonylation of the carboxylic acid double bond generates a linear aldehyde, that is, immediately
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::449ead457e806ea25ee2c09ed0bd8075
https://doi.org/10.1016/j.tet.2010.03.064
https://doi.org/10.1016/j.tet.2010.03.064
Publikováno v:
Organic Letters. 11:5314-5317
A multicomponent reaction between H(2), CO, an unsaturated carboxylic acid derivative, and binucleophiles has been discovered. This process represents a combination of diversity-oriented synthesis and multicomponent reactions including amidation and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9224d476736cad88fa137a91522395a
https://doi.org/10.1021/ol902279m
https://doi.org/10.1021/ol902279m
Publikováno v:
ChemInform. 42
A variety of substituted piperidines and 1,4-substituted indolizine (XVII) are prepared using the indium-mediated aminoallylation and -crotylation of aldehydes with 1-amino-2-indanol (I), Rh(I)-catalyzed hydroformylative cyclohydrocarbonylation, open
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28d84bd9c446bedbd5d5c6a4a93c7ee4
https://doi.org/10.1002/chin.201136147
https://doi.org/10.1002/chin.201136147
Publikováno v:
Organic letters. 13(9)
Convenient accesses to enantiomerically pure 2-, 2,3-, 2,6-, 2,3,6-substituted piperidines and 1,4-substituted indolizine are described. At first, indium-mediated aminoallylation and -crotylation of aldehydes with (R)-phenylglycinol or (1R,2S)-1-amin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d33f9f33d6db647dc3e5ba00cbe1634
https://pubmed.ncbi.nlm.nih.gov/21462951
https://pubmed.ncbi.nlm.nih.gov/21462951
Publikováno v:
ChemInform. 42
A convenient procedure is developed for domino hydroformylation cyclization reactions of unsaturated alcohols, amines and amides to produce various O- and N-containing heterocycles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba8fc0e7f7a90896725e1bc4c22f678d
https://doi.org/10.1002/chin.201117048
https://doi.org/10.1002/chin.201117048
Autor:
Jessica Salvadori, Nicolas Girard, Etienne Airiau, Marianna Pizzeti, André Mann, Maurizio Taddei
Publikováno v:
The Journal of organic chemistry. 75(24)
Linear hydroformylation of N-protected allyl- or homoallylamines (cyclohydrocarbonylation: CHC), followed by a reductive amination constitute the two key steps toward convenient routes to aza-heterocycles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a46e580ddd20ecc42d62c980a219a153
https://pubmed.ncbi.nlm.nih.gov/21082772
https://pubmed.ncbi.nlm.nih.gov/21082772
Publikováno v:
ChemInform. 41
Bicyclic, tricyclic, tetracyclic and spirocyclic oxazolo- and oxazinopiperidines are prepared by the reaction of acids (I) or (XV) with 1,2- or 1,3-amino alcohols under syngas atmosphere and microwave irradiation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86379fb04c66fd0e89ff4c748b157fef
https://doi.org/10.1002/chin.201039154
https://doi.org/10.1002/chin.201039154
Publikováno v:
ChemInform. 41
Carbonylation reaction is a very effective transformation for the synthesis of esters, amides, and heterocyclic compounds. Heterogeneous catalyzed carbonylation reactions can be carried out using the association of Pd/C and microwave dielectric heati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91aefbe91a484ae00da209017c442dec
https://doi.org/10.1002/chin.201027041
https://doi.org/10.1002/chin.201027041