The title compounds were prepared via two efficient routes. The first sequence utilized a diastereospecific triflate alkylation in the key bond forming step while the second method relied on a novel intramolecular Mitsunobu reaction to set the required stereochemistry. Many pharmaceutical agents co
Stereoselective total synthesis of (+)-(6R,2′S)-cryptocaryalactone and (−)-(6S,2′S)-epi cryptocaryalactone via asymmetric acetate aldol reaction
✍ Scribed by J.S. Yadav; Dinesh C. Bhunia; B. Ganganna
- Book ID
- 113930641
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- French
- Weight
- 432 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0040-4039
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