The Journal of organic chemistry

Synthesis of some unsymmetrical bridged terpyridines

TR Kelly, RL Lebedev

Index: Kelly, T. Ross; Lebedev, Rimma L. Journal of Organic Chemistry, 2002 , vol. 67, # 7 p. 2197 - 2205

Full Text: HTML

Citation Number: 47

Abstract

Novel unsymmetrical terpyridines 1 and 2 are synthesized using intra-and inter molecular Michael additions as the key reactions, followed by the construction of the central pyridine ring. Terpyridine 1 represents a heretofore unknown hexacyclic ring system.

Related Articles:

Synthesis of new chiral peptide nucleic acid (PNA) monomers

[Falkiewicz; Wisniowski; Kolodziejczyk; Wisniewski Nucleosides, Nucleotides and Nucleic Acids, 2001 , vol. 20, # 4-7 p. 1393 - 1397]

Synthesis of a peptide nucleic acid with a novel 1??methyl??6??mercaptopurine base

[Aboul-Fadl, Tarek; Rajeev, Gopalan; Broom, Arthur D. Journal of Heterocyclic Chemistry, 2008 , vol. 45, # 2 p. 445 - 451]

Synthesis of analogs of 1, 3-dihydroxyacetone phosphate and glyceraldehyde 3-phosphate for use in studies of fructose-1, 6-diphosphate aldolase

[Journal of Organic Chemistry, , vol. 53, # 15 p. 3457 - 3465]

Exploration of the P 1 SAR of aldehyde cathepsin K inhibitors

[Bioorganic and medicinal chemistry letters, , vol. 14, # 1 p. 275 - 278]

More Articles...