Regio- and stereochemistry of Michael addition of methanol to Thiele's ester

Acid‐promoted esterification of Thiele's acid with methanol was found to afford three products. In addition to the expected major product (i.e. the corresponding dimethyl ester, 2a), two minor products are obtained, one of which, 3, results from subsequent Michael addition of methanol to the no...

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Veröffentlicht in:	Journal of physical organic chemistry 2004-03, Vol.17 (3), p.174-179
Hauptverfasser:	Minter, David E., Smith, William B., Marchand, Alan P., Etukala, Jagan Reddy, Sivappa, Rasapalli
Format:	Artikel
Sprache:	eng
Schlagworte:	Michael reactions NMR NMR, theoretical studies polycyclic aliphatic compounds theoretical studies
Online-Zugang:	Volltext
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