The stereoselective synthetic methods for anti-and syn-fused tricyclic guanidine compounds 4a and 4b were developed based on a successive 1,3-dipolar cycloaddition. Through these synthetic studies, the stereochemistry of the left-hand tricyclic guanidine unit of batzelladine F (3) was confirmed as a
โฆ LIBER โฆ
Synthesis of the left hand unit of batzelladine F; Revision of the reported relative stereochemistry
โ Scribed by Gregory P. Black; Patrick J. Murphy; Andrew J. Thornhill; Nigel D.A. Walshe; Cinzia Zanetti
- Book ID
- 108379340
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 511 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0040-4020
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