The first application of the Baylis–Hillman reaction in azetidine chemistry: a convenient synthesis of azetidine-3-carbonitriles/carboxylates
✍ Scribed by Lal Dhar S. Yadav; Vishnu P. Srivastava; Rajesh Patel
- Book ID
- 108285117
- Publisher
- Elsevier Science
- Year
- 2008
- Tongue
- French
- Weight
- 172 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
A convenient, general and efficient synthesis of 2-methylenealkanoates and alkanenitriles is accomplished via the regioselective nucleophilic (S N 2%) addition of hydride ion from NaBH 4 to (2Z)-2-(bromomethyl)alk-2-enoates and 2-(bromomethyl)alk-2-enenitriles respectively in the presence of DABCO i
## Abstract magnified image A new route to 2__H__‐thiochromenes using the tandem S~N~2′ and S~N~Ar reaction of several Baylis‐Hillman acetates having an __ortho__‐substituent, such as a halogen or nitro group, with sodium sulfide in aqueous dimethyl sulfoxide has been described.
## Abstract magnified image A simple synthesis of several methyl 2‐oxo‐2,3‐dihydrobenzo[__b__]oxepine‐4‐carboxylates from Baylis‐Hillman adducts of __O__‐benzyl protected 2‐hydroxybenzadehydes has been described through the acetylation, cyanation, debenzylation, as well as acid assisted Pinner cyc