引用本文:
Reza heydari, Batool Tahamipour. Highly regioselective synthesis of dicyano-8a, 10,11-trihydropyrrolo[1,2-a] [1,10]phenanthrolines via a domino-Knoevenagel-cyclization[J]. Chinese Chemical Letters,
2011, 22(11): 1281-1284.
doi:
10.1016/j.cclet.2011.05.035
Citation: Reza heydari, Batool Tahamipour. Highly regioselective synthesis of dicyano-8a, 10,11-trihydropyrrolo[1,2-a] [1,10]phenanthrolines via a domino-Knoevenagel-cyclization[J]. Chinese Chemical Letters, 2011, 22(11): 1281-1284. doi: 10.1016/j.cclet.2011.05.035
Citation: Reza heydari, Batool Tahamipour. Highly regioselective synthesis of dicyano-8a, 10,11-trihydropyrrolo[1,2-a] [1,10]phenanthrolines via a domino-Knoevenagel-cyclization[J]. Chinese Chemical Letters, 2011, 22(11): 1281-1284. doi: 10.1016/j.cclet.2011.05.035
Highly regioselective synthesis of dicyano-8a, 10,11-trihydropyrrolo[1,2-a] [1,10]phenanthrolines via a domino-Knoevenagel-cyclization
摘要:
1, 10-Phenanthrolinium N-ylides, can react with malonitrile and aromatic aldehydes via a domino-Knoevenagel cyclization to afford a new class of mhydropyrrolo[l, 2-a] [l, 10]phenanthroline derivatives as stable helical compounds in a simple, mild, and efficient protocol in excellent yields.
English
Highly regioselective synthesis of dicyano-8a, 10,11-trihydropyrrolo[1,2-a] [1,10]phenanthrolines via a domino-Knoevenagel-cyclization
Abstract:
1, 10-Phenanthrolinium N-ylides, can react with malonitrile and aromatic aldehydes via a domino-Knoevenagel cyclization to afford a new class of mhydropyrrolo[l, 2-a] [l, 10]phenanthroline derivatives as stable helical compounds in a simple, mild, and efficient protocol in excellent yields.
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