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NEW STRATEGY FOR THE SYNTHESIS OF THE TAXANE DITERPENES - FORMATION OF THE 8-MEMBERED B-RING OF TAXOL BY SEMI-PINACOL REARRANGEMENT

NEW STRATEGY FOR THE SYNTHESIS OF THE TAXANE DITERPENES - FORMATION OF THE 8-MEMBERED B-RING OF TAXOL BY SEMI-PINACOL REARRANGEMENT

Dettagli Bibliografici
Autori principali: Magnus, P, Diorazio, L, Donohoe, T, Giles, M, Pye, P, Tarrant, J, Thom, S
Natura: Journal article
Pubblicazione: 1995
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Documenti analoghi

  • Taxane diterpenes .3. Formation of the eight-membered B-ring by semi-pinacol rearrangement
    di: Magnus, P, et al.
    Pubblicazione: (1996)
  • NEW STRATEGY FOR THE SYNTHESIS OF THE TAXANE DITERPENES - FORMATION OF THE BC-RINGS OF TAXOL VIA A [5+2]-PYRYLIUM YLIDE-ALKENE CYCLIZATION, RING EXPANSION STRATEGY
    di: Bauta, W, et al.
    Pubblicazione: (1995)
  • Taxane diterpenes .2. Synthesis of the 7-deoxy ABC taxane skeleton, and reactions of the A-ring
    di: Magnus, P, et al.
    Pubblicazione: (1996)
  • Taxane diterpenes .1. Control of relative and absolute stereochemistry in intramolecular pyrylium ylide-alkene cyclizations for the synthesis of taxol precursors.
    di: Bauta, W, et al.
    Pubblicazione: (1996)
  • Brönsted Acid of Keggin Type Polyoxometalate Catalyzed Pinacol Rearrangement
    di: Aldes Lesbani, et al.
    Pubblicazione: (2014-08-01)

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