Simple synthesis of α-hydroxyamino carbonyl compounds: new scope of the nitroso aldol reaction
N Momiyama, H Yamamoto
Index: Momiyama, Norie; Yamamoto, Hisashi Organic Letters, 2002 , vol. 4, # 21 p. 3579 - 3582
Full Text: HTML
Citation Number: 94
Abstract
The reaction of nitroso compounds with enolates,” the nitroso aldol reaction”, occurs in high yield to generate α-hydroxyamino carbonyl compounds. Yields range from 42% to 98% with N-selectivity> 99: 1 from commercially available aromatic or aliphatic nitroso compounds and a variety of alkali metal or tin enolates.
Related Articles:
[Momiyama, Norie; Yamamoto, Hisashi Journal of the American Chemical Society, 2005 , vol. 127, # 4 p. 1080 - 1081]
[Yanagisawa, Akira; Izumi, Youhei; Takeshita, Satoshi Synlett, 2009 , # 5 p. 716 - 719]