| Yazarlar |
Dr. Öğr. Üyesi Nuriye Tuna SUBAŞI
Türkiye |
Ayhan S Demir
|
| Özet |
| The use of L-proline to act as an organocatalyst in the aldol reaction of acylphosphonates and non enolizable aldehydes failed; however, it reacted with the aldehydes to afford azomethine ylides after decarboxylation that in turn underwent 1,3-dipolar cycloaddition with the acylphosphonates to form a bicyclic hexahydropyrrolo[1,2-c]oxazol-1-ylphosphonates in good yield. No azomethine ylide formation was observed on the reaction of acylphosphonates with proline. (C) 2017 Elsevier Ltd. All rights reserved. |
| Anahtar Kelimeler |
| Dipolar cycloaddition | Proline | Acylphosphonate | Azomethine ylide |
| Bildiri Türü | Tebliğ/Bildiri |
| Bildiri Alt Türü | Özet Metin Olarak Yayımlanan Tebliğ (Uluslararası Kongre/Sempozyum) |
| Bildiri Niteliği | Web of Science Kapsamındaki Kongre/Sempozyum |
| Bildiri Dili | İngilizce |
| Kongre Adı | 1st International Balkan Chemistry Congress (IBCC) |
| Kongre Tarihi | 17-09-2018 / 20-09-2018 |
| Basıldığı Ülke | Türkiye |
| Basıldığı Şehir | Edirne |
| Atıf Sayıları | |
| WoS | 3 |
