Zobrazeno 1 - 10
of 10
pro vyhledávání: '"N. E. Byrne"'
Publikováno v:
Tetrahedron Letters. 34:3505-3508
Benzoquinones add regioselectively to alkylidenecyclohexanes. The photoadducts are converted into useful building blocks in good yield.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::204acdf8679fb0230ce92bc9d5344699
https://doi.org/10.1016/s0040-4039(00)73621-5
https://doi.org/10.1016/s0040-4039(00)73621-5
Autor:
Marco A. Ciufolini, Z. L. Xiao, Lon J. Wilson, J. L. Margrave, R. E. Haufler, N. E. Byrne, L. P. F. Chibante, Robert H. Hauge, Michael M. Haley, Sean C. O'Brien, Y. Chai, Richard E. Smalley, Robert F. Curl, J. Conceicao, W. E. Billups, C. Pan, Scott Flanagan
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e60e74dfb2d27184d1d00f46103fc20c
https://doi.org/10.1002/chin.199112171
https://doi.org/10.1002/chin.199112171
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a085e5c8fa90cd4d1d72434ed221c81
https://doi.org/10.1002/chin.199333074
https://doi.org/10.1002/chin.199333074
Autor:
Marco A. Ciufolini, N. E. Byrne
Publikováno v:
Journal of the American Chemical Society. 113:8016-8024
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d1e590200810264cacecad11d9c61d7
https://doi.org/10.1021/ja00021a031
https://doi.org/10.1021/ja00021a031
Autor:
R. E. Haufler, J. Conceicao, L. P. F. Chibante, Y. Chai, N. E. Byrne, S. Flanagan, M. M. Haley, S. C. O'Brien, C. Pan
Publikováno v:
The Journal of Physical Chemistry. 94:8634-8636
Buckminsterfullerene, C{sub 60}, was prepared in gram quantities by contact-arc vaporization of a graphite rod in a 100-Torr atmosphere of helium, followed by extraction of the resultant graphite soot with toluene. The dominance of C{sub 60} in this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::522e9ea3911a234de8ba49c03db7ce9a
https://doi.org/10.1021/j100387a005
https://doi.org/10.1021/j100387a005
Autor:
Marco A. Ciufolini, N. E. Byrne
Publikováno v:
Tetrahedron Letters. 30:5559-5562
A sequence involving a modified Knoevenagel-Stobbe pyridine synthesis, and an unusual intramolecular reaction between a quinone and an azide, permits expeditious assembly of the ring system of the cystodytin alkaloids.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84ba9bc992a7f6bf99919837286bfecc
https://doi.org/10.1016/s0040-4039(01)93799-2
https://doi.org/10.1016/s0040-4039(01)93799-2
Publikováno v:
Journal of the American Chemical Society. 111:3473-3475
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bafb5c40c55dd939498f0f9200d4abd7
https://doi.org/10.1021/ja00191a078
https://doi.org/10.1021/ja00191a078
Publikováno v:
ChemInform. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa50f69a906bc373c5be5fbeba1686bc
https://doi.org/10.1002/chin.198933314
https://doi.org/10.1002/chin.198933314
Autor:
N. E. Byrne, Marco A. Ciufolini
Publikováno v:
ChemInform. 20
Dihydropyrans obtained by cyclocondensation of aromatic enones with vinyl ethers are transformed into pyridines by treatment with hydroxylamine hydrochloride.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb1d0cea9beb2f0a716bc1737a255a37
https://doi.org/10.1002/chin.198910218
https://doi.org/10.1002/chin.198910218
Autor:
Marco A. Ciufolini, N. E. Byrne
Publikováno v:
J. Chem. Soc., Chem. Commun.. :1230-1231
Dihydropyrans obtained by cyclocondensation of aromatic enones with vinyl ethers are transformed into pyridines by treatment with hydroxylamine hydrochloride.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6064164f6d26625a227e73006f442dc5
https://doi.org/10.1039/c39880001230
https://doi.org/10.1039/c39880001230