Formamide as an efficient nitrogen nucleophile for the Michael addition to nitroalkenes
摘要:
Secondary acyclic formamide serves as an efficient nucleophile to nitroalkenes to give corresponding Michael adducts in good yields. The nitro group in the adducts was useful for further heterocyclic synthesis. (c) 2006 Elsevier Ltd. All rights reserved.
Formamide as an efficient nitrogen nucleophile for the Michael addition to nitroalkenes
摘要:
Secondary acyclic formamide serves as an efficient nucleophile to nitroalkenes to give corresponding Michael adducts in good yields. The nitro group in the adducts was useful for further heterocyclic synthesis. (c) 2006 Elsevier Ltd. All rights reserved.
Formamide as an efficient nitrogen nucleophile for the Michael addition to nitroalkenes
作者:Akio Kamimura、Ayako Kadowaki、Yoshiaki Nagata、Hidemitsu Uno
DOI:10.1016/j.tetlet.2006.02.065
日期:2006.4
Secondary acyclic formamide serves as an efficient nucleophile to nitroalkenes to give corresponding Michael adducts in good yields. The nitro group in the adducts was useful for further heterocyclic synthesis. (c) 2006 Elsevier Ltd. All rights reserved.