Palladium(II)-Catalyzed Dicarboxymethylation of Chiral Allylic Alcohols: Chirality Transfer Affording Optically Active Diesters Containing Three Contiguous Chiral Centers

Simple item page
dc.contributor.authorOthman Hamed
dc.contributor.authorPatrick M. Henry
dc.contributor.authorDaniel P. Becker
dc.date.accessioned2017-05-03T09:36:44Z
dc.date.available2017-05-03T09:36:44Z
dc.date.issued2011-06-01
dc.description.abstract<p>Pd-catalyzed olefin dicarbonylation of chiral allylic alcohols with chirality transfer affords the chiral alcohol diesters contiguous chiral centers, in good to excellent diastereoselectivities (78- 98%).</p>en
dc.description.abstract<p>Pd-catalyzed olefin dicarbonylation of chiral allylic alcohols with chirality transfer affords the chiral alcohol diesters contiguous chiral centers, in good to excellent diastereoselectivities (78- 98%).</p>ar
dc.identifier.urihttps://hdl.handle.net/20.500.11888/9510
dc.titlePalladium(II)-Catalyzed Dicarboxymethylation of Chiral Allylic Alcohols: Chirality Transfer Affording Optically Active Diesters Containing Three Contiguous Chiral Centersen
dc.titlePalladium(II)-Catalyzed Dicarboxymethylation of Chiral Allylic Alcohols: Chirality Transfer Affording Optically Active Diesters Containing Three Contiguous Chiral Centersar
dc.typeOther
Files
Original bundle
Now showing 1 - 1 of 1
Thumbnail Image
Name:
palladiumii-catalyzed-dicarboxymethylation-chiral-allylic-alcohols-chirality-transfer-affording-opti.pdf
Size:
15.21 KB
Format:
Adobe Portable Document Format
Description:
Download
Collections
The Fifth Palestinian International Chemistry Conference