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  • Highly stereoselective, cobalt(III)-directed Mannich additions in water yielding α-methylamino acid products.

Highly stereoselective, cobalt(III)-directed Mannich additions in water yielding α-methylamino acid products.

Dalton transactions (Cambridge, England : 2003) (2012-11-22)
Stephanie Oerum, Peter Krabbe, Magnus Schau-Magnussen, Søren Furbo, Jesper Bendix, Anders Hammershøi
RESUMO

Highly stereoselective and rapid (<1 min) addition reactions to the imine double bond of 2-(methylimino)acetate complexes [L(4)Co(O(2)CCH=NCH(3))](2+) [L(4) = (en)(2) (7), (tren) (11)] were achieved in aqueous solution with nitromethane, ethyl 3-oxobutanoate or diethyl malonate. The molecular structures of two product complexes, rac-(Δ*-R(C)*-S(N)*)-[Co(en)(2)(O(2)CCH[CH(2)NO(2)]NHCH(3))]ZnCl(4) and rac-(Δ*-R(C)*-S(N)*)-[Co(en)(2)(O(2)CCH[CH(2)COCH(3)]NHCH(3))]ZnCl(4), were established by X-ray diffraction.

MATERIAIS
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Sigma-Aldrich
Nitromethane, ACS reagent, ≥95%
Sigma-Aldrich
Nitromethane, ReagentPlus®, ≥99.0%
Sigma-Aldrich
Diethyl malonate, ReagentPlus®, 99%
Sigma-Aldrich
Ethyl acetoacetate, ReagentPlus®, 99%
Sigma-Aldrich
Ethyl acetoacetate, natural, ≥97%, FG
Sigma-Aldrich
Nitromethane, suitable for HPLC, ≥96%
Sigma-Aldrich
Diethyl malonate, ≥98%, FG
Sigma-Aldrich
Ethyl acetoacetate, ≥99%, FCC, FG
Sigma-Aldrich
Ethyl acetoacetate, puriss. p.a., ≥99.0% (GC)
Sigma-Aldrich
Ethyl acetoacetate, Arxada quality, ≥99.0% (GC)