Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Mark A. Holoboski"'
Autor:
Paul R. Blakemore, Christine S. Nylund Kolz, Neal J. Green, James D. White, E Bryan Hauser, Linda E Keown, Mark A. Holoboski, Barton W. Phillips
Publikováno v:
The Journal of Organic Chemistry. 67:7750-7760
Rhizoxin D (2) was synthesized from four subunits, A, B, C, and D representing C3-C9, C10-C13, C14-C19, and C20-C27, respectively. Subunit A was prepared by cyclization of iodo acetal 21, which set the configuration at C5 of 2 through a stereoselecti
Publikováno v:
Tetrahedron Letters. 38:7333-7336
Publikováno v:
Journal of the American Chemical Society. 118:6210-6219
The first asymmetric total syntheses of (+)-1-deoxylycorine (2a) and (+)-lycorine (2b), the unnatural enantiomer of lycorine (1), are described. Construction of lactam 12, a key intermediate in the synthesis of both 2a and 2b, began by Birch reductio
Autor:
Mark A. Holoboski, Arthur G. Schultz
Publikováno v:
Tetrahedron Letters. 34:3021-3024
Cyclic β-ketoesters and β-ketoamides are converted to 2-(carbalkoxy)- and 2-(aminocarbonyl)-2-cycloalken-1-ones by treatment with Pb(OAc)4 and Cu(OAc)2 in benzene.
Publikováno v:
ChemInform. 23
Autor:
Arthur G. Schultz, Mark A. Holoboski
Publikováno v:
ChemInform. 24
Cyclic β-ketoesters and β-ketoamides are converted to 2-(carbalkoxy)- and 2-(aminocarbonyl)-2-cycloalken-1-ones by treatment with Pb(OAc)4 and Cu(OAc)2 in benzene.
Publikováno v:
ChemInform. 24
Publikováno v:
ChemInform. 24
Publikováno v:
ChemInform. 27
The first asymmetric total syntheses of (+)-1-deoxylycorine (2a) and (+)-lycorine (2b), the unnatural enantiomer of lycorine (1), are described. Construction of lactam 12, a key intermediate in the synthesis of both 2a and 2b, began by Birch reductio
Publikováno v:
ChemInform. 29