First stereoselective total synthesis of pectinolide A
โ Scribed by J.S. Yadav; S.S. Mandal
- Book ID
- 113929860
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- French
- Weight
- 367 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
The first total synthesis of Goniothalesdiol A, isolated from the stems of Goniothalamus amuyon (Annonaceae) is reported. The C2 stereocentre and C3/C4 syn diol were created by a Sharpless kinetic resolution followed by acetonide formation. The tetrahydropyran ring was formed and the C6 stereocentre
The first stereoselective total synthesis of trichodermone A using Baylis-Hillman and ring-closing metathesis (RCM) reactions as key steps is reported.
The first stereoselective total synthesis of the natural product (+)-dodoneine is described involving a Crimmins aldol reaction and a Horner-Wadsworth-Emmons olefination as the key steps.