Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Michael G. Matturro"'
Publikováno v:
Journal of the American Chemical Society. 112:5854-5861
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65d29f457fbdd8a9a4da00e58a77f263
https://doi.org/10.1021/ja00171a028
https://doi.org/10.1021/ja00171a028
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d78e6ced9305f54fd1da500715e22685
https://doi.org/10.1002/chin.199044081
https://doi.org/10.1002/chin.199044081
Autor:
Michael G. Matturro, Kenneth B. Wiberg, George J. Burgmaier, Paul J. Okarma, William P. Dailey, Mark E. Jason, William F. Bailey, Philip Warner
Publikováno v:
Tetrahedron. 42:1895-1902
The preparation of bicyclo [2.2.0]hex- 1(4)-ene ( 1 ) via ring expansion of a cyclopropylcarbene or the dehalogenation of 1-bromo-4-chlorobicyclo[2.2.0]hexane is described. It is one of the most reactive of the alkenes which may be observed at room t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d600c72e7920d51140a9ecce59c0a70d
https://doi.org/10.1016/s0040-4020(01)87609-2
https://doi.org/10.1016/s0040-4020(01)87609-2
Autor:
Mary Ann White, Casmir S. Ilenda, Michael G. Matturro, Henry E. Bryndza, Neil E. Schore, Robert G. Bergman
Publikováno v:
Journal of the American Chemical Society. 106:7451-7461
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::985fc6a1cc85eddfe56ee9cf146c697a
https://doi.org/10.1021/ja00336a026
https://doi.org/10.1021/ja00336a026
Publikováno v:
The Journal of Organic Chemistry. 50:5560-5566
Reactions within three-dimensional organic matrices are often controlled by diffusion processes. Bituminous coal was treated with a series of tetra-n-alkylammonium hydroxides (R/sub 4/NOH, R = methyl, ethyl, n-propyl, n-butyl, n-hexyl, and n-octyl) i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c46c2d9d1e38ba4a5a356855e3736d77
https://doi.org/10.1021/jo00350a026
https://doi.org/10.1021/jo00350a026
Publikováno v:
Journal of the American Chemical Society. 106:2194-2200
On prepare le compose du titre, membre le plus simple de la serie des «superphanes» par dimerisation du bicyclo [2.2.0] hexene-1(4). L'analyse RX indique une distance de 2,40 A entre les doubles liaisons. On discute le mecanisme de la dimerisation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd09a7b38f53255586862967e3b8e2a2
https://doi.org/10.1021/ja00319a047
https://doi.org/10.1021/ja00319a047
Publikováno v:
The Journal of Organic Chemistry. 47:2720-2722
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90d52633d43f1bf2312a8fe5fd1c142e
https://doi.org/10.1021/jo00135a007
https://doi.org/10.1021/jo00135a007
Autor:
Richard W. Holder, Michael G. Matturro
Publikováno v:
The Journal of Organic Chemistry. 42:2166-2168
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab8cff4cddeb3caddb595361510af919
https://doi.org/10.1021/jo00432a033
https://doi.org/10.1021/jo00432a033
Publikováno v:
Chemischer Informationsdienst. 13
The reaction of tricyclo[4.2.2.22,5]dodeca-1,5-diene with bromine gives a novel saturated dibromide with a 1,5-bridge, as determined by X-ray crystallography.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0ba8695680cf83772e3e42a1363e676
https://doi.org/10.1002/chin.198202164
https://doi.org/10.1002/chin.198202164
Autor:
Paul J. Okarma, Richard D. Adams, Brigitte E. Segmuller, Kenneth B. Wiberg, Michael G. Matturro
Publikováno v:
Chemischer Informationsdienst. 15
Determination par diffraction RX du tricyclo [4.2.2.2 2,5 ] dodecadiene-1,5. Etude de la nature des interactions entre doubles liaisons et des effets de distorsion sur les densites electroniques. Examen de l'effet de transformation des doubles liaiso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b2aeb79eabdae185a8917519d5d7c95
https://doi.org/10.1002/chin.198428057
https://doi.org/10.1002/chin.198428057