489426-11-1Relevant articles and documents
Aromatic nucleophilic substitution or CuI-catalyzed coupling route to martinellic acid
Ma, Dawei,Xia, Chengfeng,Jiang, Jiqing,Zhang, Jianhua,Tang, Wenjun
, p. 442 - 451 (2003)
Condensation of β-amino ester 8b with triflate 7 gives N-aryl amino ester 11, which is converted into 2-substituted 4-oxoquinoline 4 using an intramolecular Dieckmann reaction as the key step. CuI-mediated coupling of β-amino ester 8a with 1,4-diiodobenzene followed by an intramolecular acylation and Pd-catalyzed carbonylation provide another manner to 4. Alkylation of 4 and subsequent reductive amination deliver the cyclic imine 14, which is transformed into triamine 3 by ordinary operations. Guanylation of 3 under mild condition followed by deprotection results in the synthesis of martinellic acid 1.
