The formation of enantiomerically enriched products from chiral organolithium species is a highly efficient and selective approach for organic synthesis. [1] The majority of examples involve the selective asymmetric deprotonation of a prochiral hydrogen atom adjacent to an oxygen or nitrogen atom, s
β¦ LIBER β¦
Enantioselective Synthesis of Substituted Pyrrolidines by Dynamic Resolution
β Scribed by Iain Coldham; Samuel Dufour; Thomas F. N. Haxell; Steven Howard; Graham P. Vennall
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 71 KB
- Volume
- 114
- Category
- Article
- ISSN
- 0044-8249
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