Starting with the chiral pool compounds (-)-menthone, (-)-limonene, (-)-bet
a -pinene, and (-)-carvone, new homochiral triethanolamine derivatives were
obtained and converted to chiral silatranes. These silatranes were charact
erized by crystal structure analyses and NMR techniques. Conformational ana
lyses in the solid state and in solution show that the chiral terpene resid
ues determine the direction of the ring puckering of the silatrane moiety.