𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Studies directed toward the total synthesis of scytophycin C: Synthesis of the C(1)C(18) fragment of scytophycin C

✍ Scribed by Paul A. Grieco; Jason D. Speake


Book ID
108386496
Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
248 KB
Volume
39
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


ChemInform Abstract: Studies Directed To
✍ P. A. GRIECO; J. D. SPEAKE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

Studies Directed Toward the Total Synthesis of Scytophycin C: Synthesis of the C 1 -C 18 Fragment of Scytophycin C. -The synthesis of the C-1 to C-18 fragment (X) is based on a highly stereoselective carbon Ferrier-type rearrangement reaction of deoxyglucal (I) and the silyl enol ether (II). -(GRIEC

Total Synthesis of Scytophycin C
✍ Paterson, Ian; Watson, Christine; Yeung, Kap-Sun; Wallace, Paul A.; Ward, Richar 📂 Article 📅 1997 🏛 American Chemical Society 🌐 English ⚖ 203 KB
A stereoconvergent synthesis of the C(19
✍ J.S. Yadav; Md.Moinuddin Ahmed 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 160 KB

The C( 19) C(31) fragment of the anti-tumor macrolide, scytophycin C, was realized in a stereoconvergent manner utilizing a desymmetrization approach to create eight contiguous asymmetric centers from a common precursor.