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Erreaktibo organolitikoak sintesi asimetrikoan, aminen ...

Erreaktibo organolitikoak sintesi asimetrikoan, aminen ...

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S. Arrasate Doktorego-Tesia<br />

H 3C<br />

O<br />

H R<br />

H S<br />

O<br />

N i Pr 2<br />

OCb<br />

L* = (-)-esparteina<br />

s-BuLi/L*<br />

pentanoa,<br />

ziklohexanoa<br />

-70 o C<br />

S<br />

H 3C<br />

H 3C<br />

R<br />

O<br />

(R)<br />

(S)<br />

(+)-eldanolida<br />

O<br />

N<br />

N<br />

Li<br />

HS OCb<br />

H R<br />

OCb<br />

N<br />

Li<br />

3.7 Eskema<br />

kristalizazioa<br />

N<br />

3 etapa<br />

Ti(O i Pr) 4<br />

O<br />

H<br />

OCb<br />

OH<br />

Ti(O i Pr) 3<br />

OCb<br />

Hala ere, 3.1 Irudian adierazten diren α-oxianioi aliliko sekundarioak 29<br />

konfigurazionalki egonkorrak dira, dagozkien eratorri kiraleetatik eta TMEDA-zko<br />

baliokide baten aurrean, –70 o C-tik behera eratzen direnean.<br />

29 a) Hoppe, D. Angew. Chem. Int. Ed. Engl. 1986, 25, 160. b) Krämer, T.; Hoppe, D. Tetrahedron Lett.<br />

1987, 28, 5149. c) Hoppe, D.; Krämer, T.; Schwark, J.-R.; Zschge, O. Pure Appl. Chem. 1990, 62, 1999.<br />

74

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