“Tert-amino effect” in heterocyclic synthesis. Ring closure reactions of N,N-dialkyl-1,3-dien-1-amines
✍ Scribed by W. Verboom; D. N. Reinhoudt
- Book ID
- 104589186
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 885 KB
- Volume
- 109
- Category
- Article
- ISSN
- 0165-0513
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📜 SIMILAR VOLUMES
Palladium or nickel complex-catalyzed telomerizations of 1,3-dienes with active hydrogen compounds (carboxylic acids 1) , alcohols 11, 2) , active methylene compounds3), water4) and amines5)) h ave been reported to yield the corresponding octa-2,7-dienyl derivatives mainly. We now report the n-buty
## Abstract Addition of 9,10‐phenanthrenequinone or 3,5‐di‐__tert__‐butyl‐__o__‐benzoquinone to __N,N__‐dialkyl‐3‐alken‐1‐ynyl‐1‐amines R^2^‐CHCH‐C≡C‐NR^1^~2~ (**4**) gives quinoid α‐alkenyl‐γ‐oxo‐α,β‐unsaturated carboxamides **6** or **8**, respectively; these undergo a spontaneous ring‐closure,