Diastereoselektive Synthese von Spiro[4.5]decanonen durch intramolekulare Sakurai-Reaktionen
✍ Scribed by Dr. Dieter Schinzer
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 224 KB
- Volume
- 96
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
✦ Synopsis
Schema 1.
h, R' = COZBzl, R3 BocNH, R2, R4 = H Tabelle 1. Ausbeute und physikalische Daten der BooDerivate Za-Zj [I].
TomD Ifl a 81 (79-80/10) [s] 7.23 (t. 2H), 6.21 (t. 2H), 1.59 (s, b 85 9.5-10.S@I] 7.31(q,IH),6.82(q,lH),6.16(t,lH), (89-9110.09) 4.30 (q, 2H). 1.58 (s, 9H), 1.35 (t. 3 H) c 81 8-9 @I1 7.48 (q. lH), 7.28 (q, 1 H), 6.26 (q. 1 H), 1.58 (s, 9 H) d 94[d] 27.5-28 [h] 6.76 (d, IH), 5.89 (q, IH), 4.28 (q. 2H), 2.36 (br. s, 3 H), 1.59 (s, 9H), 1.33
📜 SIMILAR VOLUMES
**Synthesis of 3‐Dimethylamino‐3a,4,5, 7a‐tetrahydro‐1__H__‐isoindol‐1‐ones by Intramolecular __Diels‐Alder__ Reaction** Thermolysis of N^2^‐acylamidines, the acyl group of which derives from an α,β,γ,δ‐unsaturated carboxylic acid (**2, 5**–**7**), yields 3‐dimethylamino‐3a,4,5,7a‐tetrahydro‐1H‐iso