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NEW STRATEGY FOR THE SYNTHESIS...
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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
Bibliografiska uppgifter
Huvudupphovsmän:
Magnus, P
,
Diorazio, L
,
Donohoe, T
,
Giles, M
,
Pye, P
,
Tarrant, J
,
Thom, S
Materialtyp:
Journal article
Publicerad:
1995
Beståndsuppgifter
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Liknande verk
Taxane diterpenes .3. Formation of the eight-membered B-ring by semi-pinacol rearrangement
av: Magnus, P, et al.
Publicerad: (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
av: Bauta, W, et al.
Publicerad: (1995)
Taxane diterpenes .2. Synthesis of the 7-deoxy ABC taxane skeleton, and reactions of the A-ring
av: Magnus, P, et al.
Publicerad: (1996)
Taxane diterpenes .1. Control of relative and absolute stereochemistry in intramolecular pyrylium ylide-alkene cyclizations for the synthesis of taxol precursors.
av: Bauta, W, et al.
Publicerad: (1996)
Brönsted Acid of Keggin Type Polyoxometalate Catalyzed Pinacol Rearrangement
av: Aldes Lesbani, et al.
Publicerad: (2014-08-01)