Electrooxidative Cyclization of Hydroxyamino Compounds Possessing a Benzyl Group

M Okimoto, K Ohashi, H Yamamori, S Nishikawa…

Index: Synthesis, , vol. 44, # 9 p. 1315 - 1322

Full Text: HTML

Citation Number: 1

Abstract

... Synthesis 2012; 44(9): 1315-1322 DOI: 10.1055/s-0031 ... 3-dialkyl amino-1-phenylpropanones using NaBH 4 and heating to reflux in EtOH for 1–2 h (65–92%).[ 7 ] The 3-dialkyl amino-1-phenylpropanones were synthesized from 3 ... Synthesis of 1e; Typical Procedure (Table [ ...

Related Articles:

The functionalisation of electron rich aromatic compounds with 1, 3-oxazolidines and 1, 3-dimethylimidazolidine

[Heaney, Harry; Papageorgiou, George; Wilkins, Robert F. Tetrahedron, 1997 , vol. 53, # 42 p. 14381 - 14396]

Use of N-[(trimethylsilyl) methyl] amino ethers as capped azomethine ylide equivalents

[Journal of Organic Chemistry, , vol. 52, # 2 p. 235 - 244]

Formation d'ylures d'azométhine par thermolyse d'oxazolidines. Etude de la réaction en solution et en phase vapeur

[Bureau, R.; Mortier, J.; Joucla, M. Bulletin de la Societe Chimique de France, 1993 , vol. 130, p. 584 - 596]

Use of N-[(trimethylsilyl) methyl] amino ethers as capped azomethine ylide equivalents

[Journal of Organic Chemistry, , vol. 52, # 2 p. 235 - 244]

More Articles...