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Title 

An expedient synthesis of (+)-quinolactacin A2

Authors 

S J ParkK N ChoWon Gon KimK I Lee

Publisher 

Elsevier

Issue Date 

2004

Citation 

Tetrahedron Letters, vol. 45, no. 48, pp. 8793-8795

Keywords 

β-ketoester(+)-Quinolactacin A2friedl?nder-type annulationisatoic anhydridequinolactacin Aannulation reactioncarbon nuclear magnetic resonancedrug synthesishigh performance liquid chromatographyproton nuclear magnetic resonance

Abstract 

An expedient synthesis of quinolactacin A2 from N-methylisatoic anhydride and N-Boc-(2S,3S)-isoleucine has been achieved. The key step involves the Friedl?nder-type annulation of isatoic anhydride and β-ketoester derived from isoleucine.

ISSN 

0040-4039

Link 

http://dx.doi.org/10.1016/j.tetlet.2004.10.001

Appears in Collections

1. Journal Articles > Journal Articles

Registered Date

2017-04-19


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