| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271915 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
A concise approach for the total synthesis of attenols A and B is described involving MacMillan's α-aminooxylation, Evan's asymmetric alkylation, Brown's allylation, and spiro-ketalization as key steps. This approach has successfully demonstrated the α-aminooxylation protocol for the construction of the anti-1,3-diol unit.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
B.V. Subba Reddy, B. Phaneendra Reddy, N. Swapnil, J.S. Yadav,