Abstract
Perhydro-1,3-benzoxazines derived from (−)-8-amino menthol behave as masked aldehydes and chiral templates in diastereoselective intramolecular Pauson–Khand reactions with norbornene and norbornadiene. The regioselectivity is excellent for unsubstituted or methyl-substituted acetylenes and moderate with phenyl-substituted alkynes. The stereoselection is very poor or moderate depending also on the substitution pattern of both the triple bond and the perhydrobenzoxazine nucleus. The hydrolysis of the cycloadducts leads to 2- or 3-formyl–cyclopentenone derivatives.
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