1993
DOI: 10.1007/bf00781073
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Synthesis of azacyclic prostaglandin analogs (review)

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“…Three reviews published previously [7][8][9] have shown that heterocyclic prostanoids could be synthesized via different routes: a) introduction of the side chains (Rα/Rω) to the complete cyclic fragment; b) ring closure in one of the last stages of the synthesis; and c) introduction of the heteroatom into the cyclopentane ring of 11-norprostaglandins. The first route seems to have advantages, since it is possible to modify the structures of the α and ω-side chains first and then to attach them to an appropriate heterocyclic ring.…”
Section: -Synthesis and Biological Activity Of Heterocyclic Prostmentioning
confidence: 99%
“…Three reviews published previously [7][8][9] have shown that heterocyclic prostanoids could be synthesized via different routes: a) introduction of the side chains (Rα/Rω) to the complete cyclic fragment; b) ring closure in one of the last stages of the synthesis; and c) introduction of the heteroatom into the cyclopentane ring of 11-norprostaglandins. The first route seems to have advantages, since it is possible to modify the structures of the α and ω-side chains first and then to attach them to an appropriate heterocyclic ring.…”
Section: -Synthesis and Biological Activity Of Heterocyclic Prostmentioning
confidence: 99%