Shubina T, Freund M, Schenker S, Clark T, Tsogoeva S (2012)
Publication Type: Journal article
Publication year: 2012
Original Authors: Shubina TE, Freund M, Schenker S, Clark T, Tsogoeva SB
Publisher: Beilstein-Institut
Book Volume: 8
Pages Range: 1485-1498
DOI: 10.3762/bjoc.8.168
A new guanidine-thiourea organocatalyst has been developed and applied as bifunctional organocatalyst in the Michael addition reaction of diethyl malonate to trans-β-nitrostyrene. Extensive DFT calculations, including solvent effects and dispersion corrections, as well as ab initio calculations provide a plausible description of the reaction mechanism.
APA:
Shubina, T., Freund, M., Schenker, S., Clark, T., & Tsogoeva, S. (2012). Synthesis and evaluation of new guanidine-thiourea organocatalyst for the nitro-Michael reaction: Theoretical studies on mechanism and enantioselectivity. Beilstein Journal of Organic Chemistry, 8, 1485-1498. https://doi.org/10.3762/bjoc.8.168
MLA:
Shubina, Tatyana, et al. "Synthesis and evaluation of new guanidine-thiourea organocatalyst for the nitro-Michael reaction: Theoretical studies on mechanism and enantioselectivity." Beilstein Journal of Organic Chemistry 8 (2012): 1485-1498.
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