Zobrazeno 1 - 10
of 175
pro vyhledávání: '"G. M. Elsey"'
Publikováno v:
Tetrahedron Letters. 35:1075-1078
Dimethyl octamethyltricyclo[4.2.2.0 2,5 ]deca-3,7,9-triene-7,8-dicarboxylate (Cookson's diester) ( 8 ) is rearranged thermally via a double Cope reaction to its ring-degenerate isomer ( 14 ). The structure of diester ( 8 ) (indirectly) and the rearra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dc8bed346beb23ee38f069091407c2f
https://doi.org/10.1016/s0040-4039(00)79969-2
https://doi.org/10.1016/s0040-4039(00)79969-2
Publikováno v:
ChemInform. 25
Dimethyl octamethyltricyclo[4.2.2.0 2,5 ]deca-3,7,9-triene-7,8-dicarboxylate (Cookson's diester) ( 8 ) is rearranged thermally via a double Cope reaction to its ring-degenerate isomer ( 14 ). The structure of diester ( 8 ) (indirectly) and the rearra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb00bea1c03907685e0cc92c8dba4886
https://doi.org/10.1002/chin.199426102
https://doi.org/10.1002/chin.199426102
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09f07986139a456aa64fcc7b547d4bb4
https://doi.org/10.1002/chin.199433125
https://doi.org/10.1002/chin.199433125
Autor:
Gregory W. Simpson, G. M. Elsey, J. B. F. Dunstan, G. P. Savage, Edward R. T. Tiekink, Richard A. Russell
Publikováno v:
ChemInform. 29
A series of γ-substituted α-methylidene-γ-butyrolactone derivatives underwent regiospecific 1,3-dipolar cycloaddition with N-methyl-C-phenylnitrilimine. These reactions proceeded regiospecifically and with high diastereoselectivity, generally favo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::729a2988105e6e1e27dd9b3a1beba633
https://doi.org/10.1002/chin.199841048
https://doi.org/10.1002/chin.199841048
Publikováno v:
ChemInform. 21
When heated in formic acid, methyl 2-mesyloxybicyclo[2.1.1]hexane-2-carboxylate (3) ionizes significantly faster than expected and yields the rearranged isomer (6) essentially quantitatively. The latter, on the other hand, solvolyses at a much reduce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5bbfde71b7797ecff3d674ffe7d6e12
https://doi.org/10.1002/chin.199044086
https://doi.org/10.1002/chin.199044086
Publikováno v:
Zeitschrift für Kristallographie - Crystalline Materials. 211:647-648
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7b2f7618384e35280b99ba3936c153e
https://doi.org/10.1524/zkri.1996.211.9.647
https://doi.org/10.1524/zkri.1996.211.9.647
Autor:
Edward R. T. Tiekink, G. P. Savage, J. B. F. Dunstan, Gregory W. Simpson, Richard A. Russell, G. M. Elsey
Publikováno v:
Australian Journal of Chemistry. 51:499
A series of γ-substituted α-methylidene-γ-butyrolactone derivatives underwent regiospecific 1,3-dipolar cycloaddition with N-methyl-C-phenylnitrilimine. These reactions proceeded regiospecifically and with high diastereoselectivity, generally favo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::026a27f820b408ef7a9b5098e487f0ba
https://doi.org/10.1071/c97157
https://doi.org/10.1071/c97157
Autor:
Dudziak, Mary L.1
Publikováno v:
Michigan Law Review. Nov2023, Vol. 122 Issue 2, p149-205. 57p.
Publikováno v:
Australian Journal of Chemistry. 43:1231
When heated in formic acid, methyl 2-mesyloxybicyclo[2.1.1]hexane-2-carboxylate (3) ionizes significantly faster than expected and yields the rearranged isomer (6) essentially quantitatively. The latter, on the other hand, solvolyses at a much reduce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40b0fd0d77fd9a074a7dce2eef2f386c
https://doi.org/10.1071/ch9901231
https://doi.org/10.1071/ch9901231
Autor:
Farghaly, Thoraya A.1 (AUTHOR), Al-Hussain, Sami A.2 (AUTHOR), Zaki, Magdi E. A.2 (AUTHOR), Al-Qurashi, Nadia T.3 (AUTHOR), Alharbi, Salwa S.1 (AUTHOR), Muhammad, Zeinab A.4 (AUTHOR)
Publikováno v:
Polycyclic Aromatic Compounds. 2023, Vol. 43 Issue 6, p5639-5734. 96p.