| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5266179 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
Radicamine B 5 was synthesized from p-hydroxy benzaldehyde 7 stereoselectively using acid catalysed amido cyclisation with the help of neighbouring group participation (NGP). Without NGP both radicamine B 5 and its epimer 5-epi radicamine B 6 were obtained. The key steps of the synthesis are Sharpless asymmetric dihydroxylations and acid mediated amido cyclisation.
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Physical Sciences and Engineering
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Authors
Y. Jagadeesh, B. Venkateswara Rao,