Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Cara Cesario"'
Publikováno v:
Organic Letters. 11:4076-4079
Homoallylic esters are obtained in a single transformation from allyl 2,2,2-trifluoroethyl malonates by using a Pd(0) catalyst. Facile decarboxylation of allyl 2,2,2-trifluoroethyl malonates is attributed to a decrease in pK(a) compared to allyl meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fc1f076db7f8bc32b88ed813b0203ba
https://doi.org/10.1021/ol901518g
https://doi.org/10.1021/ol901518g
Autor:
Marvin J. Miller, Cara Cesario
Publikováno v:
The Journal of Organic Chemistry. 74:5730-5733
Carbocyclic uracil polyoxin C analogs are prepared from an acylnitroso-derived hetero Diels−Alder cycloadduct in fewer than nine steps. Pd(0)/InI-mediated allylation of 4-acetoxy-2-azetidinone is used to install the β-amino acid side chain at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e3898547d61e4073c9808a8f61cff49
https://doi.org/10.1021/jo900861x
https://doi.org/10.1021/jo900861x
Titanocene(III) Chloride-Mediated Reductions of Oxazines, Hydroxamic Acids, and N-Hydroxy Carbamates
Publikováno v:
The Journal of Organic Chemistry. 74:448-451
Titanocene(III) chloride (Cp(2)TiCl), generated in situ, reduces N-O bonds of various substrates in good to excellent yields (72-95%). Reactions may be performed with stoichiometric Cp(2)TiCl or with catalytic Cp(2)TiCl.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce727601d4c1907d5a9610b3a260ae19
https://doi.org/10.1021/jo802184y
https://doi.org/10.1021/jo802184y
Autor:
Neil W. Gibson, Patricia Beck, Andrew Cooke, Feng-Lei Sun, Vanessa Smith, Michael Vrkljan, Mark Bittner, Mark J. Mulvihill, Anthony Nigro, David M. Keane, Arlindo L. Castelhano, Cara Cesario, Julie L.C. Kan, David L. Emerson, Shannon L. Winski, Mary Srebernak, Christy Nillson
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 15:1669-1673
A series of [2-imidazol-1-yl-2-(6-alkoxy-naphthalen-2-yl)-1-methyl-ethyl]-dimethyl-amines were designed and synthesized as CYP26 inhibitors, serving as retinoic acid metabolic blocking agents (RAMBA's).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da526572c07626658dcb08c905b6d524
https://doi.org/10.1016/j.bmcl.2005.01.044
https://doi.org/10.1016/j.bmcl.2005.01.044
Publikováno v:
The Journal of Organic Chemistry. 69:5124-5127
The regio- and stereospecific conversion of syn- and anti-1,2-amino alcohols to their respective syn- and anti-1,2-imidazolylpropylamines via treatment with 1,1'-carbonyldiimidazole is described. The rationale behind the regio- and stereospecific nat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94c794ba4a3bd5928ad98dc61750261e
https://doi.org/10.1021/jo049677l
https://doi.org/10.1021/jo049677l
Autor:
Cara Cesario, Marvin J. Miller
Publikováno v:
Tetrahedron Letters. 51:3050-3052
A formyl equivalent was generated in situ from Eschenmoser’s salt in aqueous THF and was reacted with an allylindium species. Acylnitroso-derived hetero-Diels Alder adducts and related allyl acetates were shown to be substrates for Pd(0)/InI-mediat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7898533c360a01885d3ce80269ba7a13
https://doi.org/10.1016/j.tetlet.2010.04.007
https://doi.org/10.1016/j.tetlet.2010.04.007
Publikováno v:
Tetrahedron letters. 51(23)
Carbocyclic aminonucleosides and epi-4′-carbocyclic puromycin were prepared from an acylnitroso-derived hetero Diels–Alder cycloadduct. Pd(0)/InI-mediated allylations of a formyl species were used to install the 4′-hydroxymethyl group. A tether
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca196410865db25b2838162a4fe45428
https://pubmed.ncbi.nlm.nih.gov/20640052
https://pubmed.ncbi.nlm.nih.gov/20640052
Publikováno v:
ChemInform. 40
Titanocene(III) chloride (Cp(2)TiCl), generated in situ, reduces N-O bonds of various substrates in good to excellent yields (72-95%). Reactions may be performed with stoichiometric Cp(2)TiCl or with catalytic Cp(2)TiCl.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b3cb4c80d62d7d7a3866177ad5e5845
https://doi.org/10.1002/chin.200919037
https://doi.org/10.1002/chin.200919037
Autor:
Cara Cesario, Marvin J. Miller
Publikováno v:
Organic letters. 11(6)
Acylnitroso-derived hetero-Diels-Alder cycloadducts are susceptible to C-O bond cleavage with Pd(0) and InI to form allylic indium(III) species. The in situ prepared allylindium compounds readily react at room temperature with Eschenmoser's salt. All
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d1415e769ad4ae2fce25a362474b40a
https://pubmed.ncbi.nlm.nih.gov/19216521
https://pubmed.ncbi.nlm.nih.gov/19216521
