📜[(R)-1-(4-Chloro-Phenyl)-3-Oxo-3-((1R,2R,4R)-1,7,7-Trimethyl-2-Trimethylsilanyloxy-Bicyclo[2.2.1]Hept-2-yl)-Propyl]-Carbamic Acid Tert-Butyl Ester置于ammonium Cerium(Iv) Nitrate体系中,用 乙腈 作为反应溶剂,化学反应 16.0H,反应生成 (R)-Boc-4-氯苯基-Beta-苯丙氨酸
参考文献:α-Oxymethyl Ketone Enolates For The Asymmetric Mannich Reaction. From Acetylene Andn-Alkoxycarbonylimines Toβ-Amino Acids
标题:α-Oxymethyl Ketone Enolates For The Asymmetric Mannich Reaction. From Acetylene Andn-Alkoxycarbonylimines Toβ-Amino Acids
摘要:
DOI:10.1002/(Sici)1521-3773(20000317)39:6<1063::Aid-Anie1063>3.0.Co;2-Y