Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jeffery Zablocki"'
Autor:
Heidi Rath Hope, Deborah Heuvelman, Kevin Duffin, Christine Smith, Jeffery Zablocki, Roger Schilling, Shridhar Hegde, Len Lee, Bryan Witherbee, Mark Baganoff, Can Bruce, Alan R. Tall, Elaine Krul, Kevin Glenn, Daniel T. Connolly
Publikováno v:
Journal of Lipid Research, Vol 41, Iss 10, Pp 1604-1614 (2000)
SC-71952, a substituted analog of dithiobisnicotinic acid dimethyl ester, was identified as a potent inhibitor of cholesteryl ester transfer protein (CETP). When tested in an in vitro assay, the concentration of SC-71952 required for half-maximal inh
Externí odkaz:
https://doaj.org/article/cc5033ac3088478fbe63f90dab676d71
Autor:
Larry E. Overman, Jeffery Zablocki, Matthew J. Sharp, Christian Caderas, Michael H. Rabinowitz, Renee M. Lett, Leslie A. Robinson
Publikováno v:
Journal of the American Chemical Society. 118:9073-9082
A concise, stereocontrolled strategy for the total synthesis of allopumiliotoxin A alkaloids is described. A much improved second generation total synthesis of enantiopure (+)-allopumiliotoxin 267A (3) was accomplished in 10 steps and 11% overall yie
Autor:
Leslie A. Robinson, Jeffery Zablocki, Michael H. Rabinowitz, Matthew J. Sharp, Nan-Horng Lin, Larry E. Overman
Publikováno v:
ChemInform. 28
A practical route for the total synthesis of pumiliotoxin A alkaloids is described. The central step is formation of the piperidine ring and establishment of the (Z)-alkylidene side chain by an iodide-promoted iminium ion−alkyne cyclization. The to
Autor:
Christian Caderas, Michael H. Rabinowitz, Jeffery Zablocki, Renee M. Lett, Larry E. Overman, Leslie A. Robinson, Matthew J. Sharp
Publikováno v:
ChemInform. 28
A concise, stereocontrolled strategy for the total synthesis of allopumiliotoxin A alkaloids is described. A much improved second generation total synthesis of enantiopure (+)-allopumiliotoxin 267A (3) was accomplished in 10 steps and 11% overall yie
Publikováno v:
ChemInform. 23
Publikováno v:
Journal of the American Chemical Society. 114:368-369
Publikováno v:
Tetrahedron Letters. 29:6541-6544
The title reaction can be employed to assemble the allopumiliotoxin A alkaloid skeleton with either stereochemistry of the C-7 allylic hydroxyl groxyl group.
Publikováno v:
ChemInform. 20