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Erreaktibo organolitikoak sintesi asimetrikoan, aminen ...

Erreaktibo organolitikoak sintesi asimetrikoan, aminen ...

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S. Arrasate Doktorego-Tesia<br />

124<br />

H 3CO<br />

Cl<br />

OCH 3<br />

Br<br />

O<br />

Br<br />

O<br />

Cl<br />

Ph<br />

Cl<br />

n-BuLi, THF<br />

-50 o C i.t.<br />

n-BuLi, THF<br />

-50 o C i.t.<br />

Cl<br />

4.29 Eskema<br />

OCH 3<br />

H 3CO O Ph<br />

Cl<br />

es > %99<br />

Teprowastina E<br />

O<br />

es > %99<br />

Cl<br />

(R)-4,6-dikloroflabanoa<br />

Prozedura hau beste bentzofuranoen <strong>sintesi</strong>an aplikatu da, enantiomerikoki<br />

puruak diren dagozkien aril bromuroetatik abiatuz. Hauek, erraz lor daitezke<br />

komertzialak diren halopropanolekin emandako 2-bromofenolen Mitsunobu<br />

erreakzioaren bidez edo zetona prokiralen erredukzio asimetrikoa dela medio (4.30<br />

Eskema). 40,39<br />

R 1<br />

Br<br />

X<br />

n-BuLi, THF<br />

R2 O R<br />

-50oC i.t.<br />

O<br />

R3 R3 R2 R1 = H; R2 = H; R3 = H; R = Ph; X = Cl<br />

R1 = H; R2 = H; R3 = H; R = Me; X = Br<br />

R1 = Me; R2 = H; R3 = H; R = Ph; X = Cl<br />

R1 =Cl; R2 = H; R3 = H; R = Ph; X = Cl<br />

es > %99<br />

4. 30 Eskema<br />

R 1<br />

R

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