Synlett

Synthesis of Novel Annulated Hymenialdisine Analogues via Palladium-Catalyzed Cross-Coupling Reactions with Aryl Boronic Acids

N Mangu, A Spannenberg, M Beller, MK Tse

Index: Mangu, Naveenkumar; Spannenberg, Anke; Beller, Matthias; Tse, Man-Kin Synlett, 2010 , # 2 p. 211 - 214

Full Text: HTML

Citation Number: 4

Abstract

Nevertheless, with the key building block 8 in hand, we envisioned the synthesis of novel hymenialdisine analogues following standard Suzuki coupling protocols. [¹6] Treatment of 8 with 4-methoxyphenyl boronic acid (1.1 equiv) in the presence of Pd(PPh 3 ) 4 (1 mol%) and aqueous sodium carbonate (2 M) as base in a mixture of toluene and ethanol (1:1) at 70 ˚C for 12-16 h, gave the desired product along with minor amounts of the deprotected compound 9a (R = ...

Related Articles:

Potent inhibition of checkpoint kinase activity by a hymenialdisine-derived indoloazepine

[Sharma, Vasudha; Tepe, Jetze J. Bioorganic and Medicinal Chemistry Letters, 2004 , vol. 14, # 16 p. 4319 - 4321]

New synthetic protocols for the preparation of unsymmetrical bisindoles

[Kaiser, Hanns Martin; Lo, Wei Fun; Riahi, Abdol Majid; Spannenberg, Anke; Beller, Matthias; Tse, Man Kin Organic Letters, 2006 , vol. 8, # 25 p. 5761 - 5764]

New synthetic protocols for the preparation of unsymmetrical bisindoles

[Kaiser, Hanns Martin; Lo, Wei Fun; Riahi, Abdol Majid; Spannenberg, Anke; Beller, Matthias; Tse, Man Kin Organic Letters, 2006 , vol. 8, # 25 p. 5761 - 5764]

More Articles...