
Tetrahedron Letters p. 2657 - 2660 (1982)
Update date:2022-08-05
Topics:
Kuroda, Shigeyasu
Kitatani, Kazuto
Ojima, Juro
Title fulvenes were synthesized through the reaction of the large-membered annulenones with diphenylketene, and examination of (1)H-NMR spectra suggests that the fulvenes are atropic.
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Doi:10.1246/cl.1982.1081
(1982)Doi:10.1139/v82-367
(1982)Doi:10.1021/jm050257d
(2005)Doi:10.1248/cpb.39.752
(1991)Doi:10.1246/cl.1982.1017
(1982)Doi:10.1007/s11164-012-0792-6
(2013)