Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Matthew P. Huisenga"'
Autor:
Wayland E. Noland, Neil J. Kroll, Matthew P. Huisenga, Ruixian A. Yue, Simon B. Lang, Nathan D. Klein, Kenneth J. Tritch
Publikováno v:
Acta Crystallographica Section E, Vol 70, Iss 12, Pp 550-554 (2014)
The title tetrone compound, C32H22N2O4S· 0.5C8H10, is the major product (50% yield) of an attempted Diels–Alder reaction of 2-(α-styryl)thiophene with N-phenylmaleimide (2 equivalents) in toluene. Recrystallization of the resulting powder from p-
Externí odkaz:
https://doaj.org/article/91ffe30add3546529f29c4f8db566a56
Autor:
Diane T. Vo, Kenny Xiong, John A. Rosenow, Nathan D. Klein, Steven P. Daniels, Jidapa Ratanayanon, Ruixian A. Yue, Neil J. Kroll, Wayland E. Noland, Matthew P. Huisenga, Hoyeon Kim, Nathan S. Duncan, Jacob K. Riley, Benjamin Johnson, Ryan J. Herzig, Kenneth J. Tritch, Andrei Nesmelov, Bee K. Ong, Simon B. Lang
Publikováno v:
Journal of Heterocyclic Chemistry. 55:2698-2714
Autor:
Matthew P. Huisenga, Kenneth J. Tritch, Simon B. Lang, Nathan D. Klein, Neil J. Kroll, Wayland E. Noland, Ruixian A. Yue
Publikováno v:
Acta Crystallographica Section E: Structure Reports
Acta Crystallographica Section E, Vol 70, Iss 12, Pp 550-554 (2014)
Acta Crystallographica Section E, Vol 70, Iss 12, Pp 550-554 (2014)
A novel meso bicyclo[2.2.2]octene-based compound was obtained from an attempted Diels–Alder reaction. It crystallizes from p-xylene as a hemisolvate.
The title tetrone compound, C32H22N2O4S· 0.5C8H10, is the major product (50% yield) of a
The title tetrone compound, C32H22N2O4S· 0.5C8H10, is the major product (50% yield) of a