Scribd Logo
Upload

Welcome to Scribd!

  • Reserpine

    Uploaded by

    Kiệt Lý
    10 views1 page
    Reserpine is a compound synthesized in 1989 using a total synthesis route. The synthesis builds the tetracyclic carbon skeleton through a Diels-Alder reaction to form ring B from intermediate A. It then uses a one-step oxidation to transform intermediate E to F.

    Original Description:

    Original Title

    BT9

    Copyright

    © © All Rights Reserved

    Available Formats

    PDF, TXT or read online from Scribd

    Did you find this document useful?

    Is this content inappropriate?

    Report this Document
    Reserpine is a compound synthesized in 1989 using a total synthesis route. The synthesis builds the tetracyclic carbon skeleton through a Diels-Alder reaction to form ring B from intermediate A. It then uses a one-step oxidation to transform intermediate E to F.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Flag for inappropriate content
    10 views1 page

    Reserpine

    Uploaded by

    Kiệt Lý
    Reserpine is a compound synthesized in 1989 using a total synthesis route. The synthesis builds the tetracyclic carbon skeleton through a Diels-Alder reaction to form ring B from intermediate A. It then uses a one-step oxidation to transform intermediate E to F.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Flag for inappropriate content
    of 1

    Reserpine

    Reserpine is an interesting compound which was synthesized by Stork in 1989. The total
    synthesis (shown below) uses a pericyclic reaction to build the carbon skeleton

    Hints:
    ● B is tetracyclic
    ● E → F involves two named oxidation reactions occurring in the same step.
    ● Optional Hint: SM→A involves alpha deprotonation and A→ B is a diels alder reaction

    Draw the structures of A - J.

    You might also like