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Volumn 55, Issue 12, 2016, Pages 4049-4053

Bioisosteric Exchange of C sp 3 -Chloro and Methyl Substituents: Synthesis and Initial Biological Studies of Atpenin A5 Analogues

Author keywords

antifungal agents; atpenins; bioisosterism; chlorinated natural products; inhibition of respiratory chain

Indexed keywords

CHAINS; FUNGICIDES;

EID: 84960416049     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201511672     Document Type: Article
Times cited : (19)

References (88)
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    • The effects of side-chain modification on binding interactions and physicochemical properties of the atpenins are not entirely clear at this point. Further studies are required to definitively establish the role of the side-chain in the atpenin scaffold. For a study on co-crystallization of succinate-ubiquinone reductase with atpenin A5 and structural analysis of the binding site, see.
    • The effects of side-chain modification on binding interactions and physicochemical properties of the atpenins are not entirely clear at this point. Further studies are required to definitively establish the role of the side-chain in the atpenin scaffold. For a study on co-crystallization of succinate-ubiquinone reductase with atpenin A5 and structural analysis of the binding site, see:, R. Horsefield, V. Yankovskaya, G. Sexton, W. Whittingham, K. Shiomi, S. Omura, B. Byrne, G. Cecchini, S. Iwata, J. Biol. Chem. 2006, 281, 7309.
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    • For an example of the use of this auxiliary in a similar process, see:, J. Zhang, et al., Tetrahedron Lett. 2009, 50, 1167.
    • (2009) Tetrahedron Lett. , vol.50 , pp. 1167
    • Zhang, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.