| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218525 | Tetrahedron | 2012 | 6 Pages |
Abstract
The development of axially chiral dicarboxylic acid catalyzed desymmetrizing asymmetric semipinacol rearrangement of symmetrically substituted six-membered cyclic β-hydroxy-α-diazo esters is reported as a means to give chiral cycloheptanones with good enantioselectivities.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
