72479-04-0Relevant articles and documents
A triply convergent total synthesis of a symchiral pyrrolidine-fused prostacyclin analog
Smith,Fuchs
, p. 2692 - 2703 (2007/10/02)
The synthesis of symchiral 1-azatricyclo[6.3.0.0]undeca-5-enyl prostaglandin I2 analog 34 is reported. Construction of the tricyclic skeleton of 34 was accomplished in two steps by employing a triply convergent approach which utilized vinyl sulfone technology. Introduction of the heterocyclic subunit of 34 was achieved by an S(N)2'-thio-Claisen rearrangement which efficiently coupled a thiolactam moiety to a suitable allylic vinyl sulfone. Annulation of bicyclic vinyl sulfones 20, 23, and 29 was accomplished via a conjugate addition of lithium acetylide 11 to the vinyl sulfone moieties, followed by an intramolecular S(N)2 displacement of a suitable nucleofuge. Competition between intramolecular carbon alkylation and β-elimination of stabilized nitrogen anions from intermediate α-sulfonyl anions 20-i, 23-i, 29-i was discussed. Refunctionalization of the resulting tricyclic skeleton was accomplished by employing standard literature protocols. Compound 34 was found to be essentially inactive as an inhibitor of collagen-induced platelet aggregation, having an IC50 of >10 μM.
Synthesis of (S)-5-substituted 4-aminopentanoic acids: A new class of γ-aminobutyric acid transaminase inactivators
Silverman,Levy
, p. 815 - 818 (2007/10/02)
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