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