NEW STRATEGY FOR THE SYNTHESIS OF THE TAXANE DITERPENES - FORMATION OF THE 8-MEMBERED B-RING OF TAXOL BY SEMI-PINACOL REARRANGEMENT
Autors principals: | Magnus, P, Diorazio, L, Donohoe, T, Giles, M, Pye, P, Tarrant, J, Thom, S |
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Format: | Journal article |
Publicat: |
1995
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Ítems similars
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Taxane diterpenes .3. Formation of the eight-membered B-ring by semi-pinacol rearrangement
per: Magnus, P, et al.
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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
per: Bauta, W, et al.
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Taxane diterpenes .2. Synthesis of the 7-deoxy ABC taxane skeleton, and reactions of the A-ring
per: Magnus, P, et al.
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Taxane diterpenes .1. Control of relative and absolute stereochemistry in intramolecular pyrylium ylide-alkene cyclizations for the synthesis of taxol precursors.
per: Bauta, W, et al.
Publicat: (1996) -
Brönsted Acid of Keggin Type Polyoxometalate Catalyzed Pinacol Rearrangement
per: Aldes Lesbani, et al.
Publicat: (2014-08-01)