Tetrahedron Letters p. 3355 - 3358 (1980)
Update date:2022-09-26
Topics:
Demailly, Gilles
Solladie, Guy
The acid-catalyzed cyclization of the chiral aldimine prepared from trans-5,9 dimethyldeca-5,9-dienal and (-)S-α-phenyl-ethylamine affords diastereoisomeric amino-5 dimethyl-2,9 octalines, the asymmetric induction being 65 percent in the trans-trans series and 35 percent in the cis-trans series.
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Doi:10.1002/ardp.19813140112
(1981)Doi:10.1021/jo00330a043
(1981)Doi:10.1007/BF02464370
(1997)Doi:10.1271/bbb.120925
(2013)Doi:10.1016/0040-4039(81)80004-4
(1981)Doi:10.1016/S0040-4020(01)97718-X
(1981)
