A synthetic approach to the polysubstituted pyran core and amide side chain of psymberin (irciniastatin A) using stereoselective organoboron methodology is described. An advanced oxyranyl pyran intermediate was prepared using a catalytic enantioselective and diastereoselective three-component reacti
โฆ LIBER โฆ
Configuration of the Psymberin Amide Side Chain
โ Scribed by Kiren, Sezgin; Williams, Lawrence J.
- Book ID
- 120337218
- Publisher
- American Chemical Society
- Year
- 2005
- Tongue
- English
- Weight
- 91 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1523-7060
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Synthetic studies toward the pyran core
โ
Hugo Lachance; Olivier Marion; Dennis G. Hall
๐
Article
๐
2008
๐
Elsevier Science
๐
French
โ 205 KB
The Stereochemical Configuration of the
โ
Jones, R. Norman
๐
Article
๐
1950
๐
American Chemical Society
๐
English
โ 236 KB
Configurations of Polypeptide Chains wit
โ
Linus Pauling and Robert B. Corey
๐
Article
๐
1952
๐
National Academy of Sciences
๐
English
โ 315 KB
Side-Chain Amination during the Reaction
โ
Reinecke, Manfred; Adickes, H. Wayne; Pyun, Chongsuh
๐
Article
๐
1971
๐
American Chemical Society
๐
English
โ 294 KB
Solvent Exchange Rates of Side-chain Ami
โ
Ponni Rajagopal; Bryan E. Jones; Rachel E. Klevit
๐
Article
๐
1998
๐
Springer Netherlands
๐
English
โ 178 KB
Solid-phase synthesis of amino amides an
โ
William L Scott; Francisca Delgado; Karen Lobb; Richard S Pottorf; Martin J O'Do
๐
Article
๐
2001
๐
Elsevier Science
๐
French
โ 86 KB
Unnatural amino amides and peptide amides can be synthesized, using solid-phase chemistry, from glycine attached directly (or through an intervening peptide sequence) to a Rink resin. The glycine is converted to an activated benzophenone imine derivative, followed by C-alkylation and hydrolysis. Thi