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Synlett 1999; 1999(4): 426-428
DOI: 10.1055/s-1999-2644
DOI: 10.1055/s-1999-2644
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data processing and storage.Stereocontrolled Synthesis of (1R,3R,4S)- and (1S,3R,4S)-3,4-diaminocyclopentanols
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Publikationsverlauf
Publikationsdatum:
31. Dezember 1999 (online)

Cis-syn and cis-anti-3,4-diaminocyclopentanols have been synthesized from cyclopentadiene in eight steps. The key transformations involved construction of benzyl ether protected cis-diazidocyclopentanols, and sequential reduction and hydrogenolysis to the unprotected diaminocyclopentanols.
stereocontrolled synthesis - vicinal diamine - diaminocyclopentanol - diazide reduction - debenzylation