Mukaiyama diastereoismers pattern by computational studies

Mukaiyama diastereoismers pattern by computational studies

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

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.

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.

Palavras-chave:

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

Referências bibliográficas

• [1] 1Parentely, A.; Moreau, X, Campagne, J.-M. Chem. Rev. 2006,106, 911.

Como citar:

Martins, João B. L.; Murta, M. M.; Resck, I. S.; dos Santos, M. L.; wagner wendell cruz dos santos santos; "Mukaiyama diastereoismers pattern by computational studies", p-237-237. In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 1, Setembro.2013. São Paulo: Blucher, 2013.
ISSN 23184043, DOI 10.5151/chempro-14bmos-R0237-1