Highly stereoselective and efficient synthesis of the dopa analogue in pepticinnamin E via enantioselective hydrogenation of dehydroamino acids
作者:DEQUN SUN
DOI:10.3906/kim-0904-14
日期:——
An efficient and new method was developed to prepare the dopa analogue 11 in natural pepticinnamin via catalytic hydrogenation of dehydroamino acids (DDAA) with a good yield and ee. Product 11 is a key intermediate towards the total synthesis of pepticinnamin E and its analogues.
本研究开发了一种高效的新方法,通过脱氢氨基酸(DDAA)的催化加氢反应制备天然肽肉桂酸中的多巴类似物 11,并取得了良好的产率和ee值。 产物 11 是全合成肽肉桂素 E 及其类似物的关键中间体。
Sun, De-Qun; Sun, Li; Luo, Min, Asian Journal of Chemistry, 2012, vol. 24, # 4, p. 1731 - 1734
作者:Sun, De-Qun、Sun, Li、Luo, Min
DOI:——
日期:——
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