The title compound, C 13 H 15 NO 3 , contains a chiral cisdisubstituted oxazine linked to a phenyl ring at the C-2 atom. The racemic crystal structure is stabilized by both intra-and intermolecular C-HÁ Á ÁO hydrogen bonds.
Stereoselective total synthesis of (+)-strictifolione and (6R)-6[(E,4R,6R)-4,6-dihydro-10-phenyl-1-decenyl)-5,6-dihydro-2H-2-pyrone
✍ Scribed by Biswanath Das; Boyapati Veeranjaneyulu; Penagaluri Balasubramanyam; Malampati Srilatha
- Book ID
- 108284640
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 599 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0957-4166
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📜 SIMILAR VOLUMES
## Abstract The stereoselective total synthesis of an antiproliferative and antifungal __α__‐pyrone natural product (6__S__)‐5,6‐dihydro‐6‐[(2__R__)‐2‐hydroxy‐6‐phenylhexyl]‐2__H__‐pyran‐2‐one is described. The key steps involved are the __Prins__ cyclization, __Mitsunobu__ reaction, and ring‐closi
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