Journal of Organic Chemistry p. 4963 - 4968 (1983)
Update date:2022-08-05
Topics:
Todesco, R.
Bockstaele, D. Van
Gelan, J.
Martens, H.
Put, J.
Schryver, F. C. De
Intramolecular excimer formation in a series of phenyl-substituted 1,3-propanediols, compounds in which the motions of the linking chain are restricted by intramolecular hydrogen bonding, was investigated under stationary conditions in n-hexane.The excime
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Doi:10.1080/104265090968451
(2006)Doi:10.1016/0022-328X(83)85055-4
(1983)Doi:10.1055/s-0033-1340959
(2014)Doi:10.1002/adsc.200404286
(2005)Doi:10.1016/j.tetlet.2005.10.034
(2005)Doi:10.1007/BF01230591
(1952)
