Synthesis of the ABH rings of ecteinascidin 597 using a connective Pummerer-type cyclisation

Laura H S Smith, Trung Thanh Nguyen, Helen F. Sneddon, David J. Procter

    Research output: Contribution to journalArticlepeer-review

    Abstract

    A connective Pummerer-type cyclisation involving a cysteine derivative and an N-benzyl glyoxamide 3 has been applied in an asymmetric synthesis of the protected ABH rings 2 of the antitumour and antimicrobial natural product ecteinascidin 597. © 2011 The Royal Society of Chemistry.
    Original languageEnglish
    Pages (from-to)10821-10823
    Number of pages2
    JournalChemical Communications
    Volume47
    Issue number38
    DOIs
    Publication statusPublished - 14 Oct 2011

    Fingerprint

    Dive into the research topics of 'Synthesis of the ABH rings of ecteinascidin 597 using a connective Pummerer-type cyclisation'. Together they form a unique fingerprint.

    Cite this