Setembro 2013 vol. 1 num. 1 - Brazilian Meeting on Organic Synthesis 2011

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Mukaiyama diastereoismers pattern by computational studies

Santos, W. W. C. ; Martins, João B. L. ; Murta, M. M. ; Resck, I. S. ; dos Santos, M. L. ;

Abstract:

Ring-closing reaction is a critical step in the synthesis of macrocyclic compounds due to entropic and enthalpic factors, associated with transition states direct cyclization in generally is not possible without activation. Our efforts to obtain zearalenone analogues from anacardic acid, have led us to explore some classical macrocyclization methods.

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Palavras-chave: Macrocyclization, diastereoisomers, zearalenone analogues,

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DOI: 10.5151/chempro-14bmos-R0237-1

Referências bibliográficas
  • [1] 1Parentely, A.; Moreau, X, Campagne, J.-M. Chem. Rev. 2006,106, 91
Como citar:

Santos, W. W. C.; Martins, João B. L.; Murta, M. M.; Resck, I. S.; dos Santos, M. L.; "Mukaiyama diastereoismers pattern by computational studies", p. 237 . In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 1, Setembro.2013. São Paulo: Blucher, 2013.
ISSN 2318-4043, DOI 10.5151/chempro-14bmos-R0237-1

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