Biomimetic Organocatalytic C–C-Bond Formations
113
Enders D, Breuer K, Raabe G, Simonet J, Ghanimi A, Stegmann HB, Teles JH
(1997b) A stable carbene as π-acceptor. Electrochemical reduction to the
radical anion. Tetrahedron Lett 38:2833
Enders D, Oberbörsch S, Adam J (2000) a-Silyl controlled asymmetric Mannich
reactions of acyclic ketones with imines. Synlett 2000:644–646
Enders D, Faure S, Potthoff M, Runsink J (2001) Diastereoselective electrophilic
fluorination of enantiopure α-silylketones using N-fluoro-benzosulfonimide: regio- and enantioselective synthesis of α-fluoroketones. Synthesis
2001:2307–2319
Enders D, Voith M, Ince SD (2002a) Preparation and reactions of 2,2-dimethyl1,3-dioxan-5-one-SAMP-hydrazone: a versatile chiral dihydroxyacetone
equivalent. Synthesis 2002:1775–1779
Enders D, Adam J, Oberbörsch S, Ward D (2002b) Asymmetric Mannich
reactions by α-silyl controlled aminomethylation of ketones. Synthesis
2002:2737–2748
Enders D, Breuer K, Kallfass U, Balensiefer T (2003) Preparation and application of 1,3,4-triphenyl-4,5-dihydro-1H-1,2,4-triazol-5-ylidene, a stable carbene. Synthesis 2003:1292–1295
Enders D, Voith M, Lenzen A (2005a) The dihydroxyacetone unit—a versatile
C3 building block in organic synthesis. Angew Chem Int Ed Engl 44:1304
Enders D, Grondal C, Vrettou M, Raabe G (2005b) Direct organocatalytic de
novo synthesis of carbohydrates. Angew Chem Int Ed Engl 44:4079
Enders D, Paleek J, Grondal C (2006a) A direct organocatalytic entry to sphingoids: asymmetric synthesis of D-arabino- and L-ribo-phytosphingosine.
Chem Commun 2006:655–657
Enders D, Grondal C, Vrettou M (2006b) Efficient entry to amino sugars and
derivatives via asymmetric organocatalytic Mannich reactions. Synthesis
2006:3597
Enders D, Niemeier O, Balensiefer T (2006c) Asymmetric intramolecular crossed-benzoin reactions by N-heterocyclic carbene catalysis. Angew Chem
Int Ed Engl 45:1463
Enders D, Niemeier O, Raabe G (2006d) Asymmetric synthesis of chromanones
via N-heterocyclic carbene catalyzed intramolecular crossed-benzoin reactions. Synlett 2006:2431
Enders D, Grondal C, Hüttl MRM (2007a) Asymmetric Organocatalytic Domino Reactions. Angew Chem Weinheim Bergstr Ger 119:1590
Enders D, Hüttl MRM, Runsink J, Raabe G, Wendt B (2007b) Organocatalytic
one pot asymmetric synthesis of functionalized tricyclic carbon skeletons
via a triple cascade/Diels-Alder sequence. Angew Chem 119:471
113
Enders D, Breuer K, Raabe G, Simonet J, Ghanimi A, Stegmann HB, Teles JH
(1997b) A stable carbene as π-acceptor. Electrochemical reduction to the
radical anion. Tetrahedron Lett 38:2833
Enders D, Oberbörsch S, Adam J (2000) a-Silyl controlled asymmetric Mannich
reactions of acyclic ketones with imines. Synlett 2000:644–646
Enders D, Faure S, Potthoff M, Runsink J (2001) Diastereoselective electrophilic
fluorination of enantiopure α-silylketones using N-fluoro-benzosulfonimide: regio- and enantioselective synthesis of α-fluoroketones. Synthesis
2001:2307–2319
Enders D, Voith M, Ince SD (2002a) Preparation and reactions of 2,2-dimethyl1,3-dioxan-5-one-SAMP-hydrazone: a versatile chiral dihydroxyacetone
equivalent. Synthesis 2002:1775–1779
Enders D, Adam J, Oberbörsch S, Ward D (2002b) Asymmetric Mannich
reactions by α-silyl controlled aminomethylation of ketones. Synthesis
2002:2737–2748
Enders D, Breuer K, Kallfass U, Balensiefer T (2003) Preparation and application of 1,3,4-triphenyl-4,5-dihydro-1H-1,2,4-triazol-5-ylidene, a stable carbene. Synthesis 2003:1292–1295
Enders D, Voith M, Lenzen A (2005a) The dihydroxyacetone unit—a versatile
C3 building block in organic synthesis. Angew Chem Int Ed Engl 44:1304
Enders D, Grondal C, Vrettou M, Raabe G (2005b) Direct organocatalytic de
novo synthesis of carbohydrates. Angew Chem Int Ed Engl 44:4079
Enders D, Paleek J, Grondal C (2006a) A direct organocatalytic entry to sphingoids: asymmetric synthesis of D-arabino- and L-ribo-phytosphingosine.
Chem Commun 2006:655–657
Enders D, Grondal C, Vrettou M (2006b) Efficient entry to amino sugars and
derivatives via asymmetric organocatalytic Mannich reactions. Synthesis
2006:3597
Enders D, Niemeier O, Balensiefer T (2006c) Asymmetric intramolecular crossed-benzoin reactions by N-heterocyclic carbene catalysis. Angew Chem
Int Ed Engl 45:1463
Enders D, Niemeier O, Raabe G (2006d) Asymmetric synthesis of chromanones
via N-heterocyclic carbene catalyzed intramolecular crossed-benzoin reactions. Synlett 2006:2431
Enders D, Grondal C, Hüttl MRM (2007a) Asymmetric Organocatalytic Domino Reactions. Angew Chem Weinheim Bergstr Ger 119:1590
Enders D, Hüttl MRM, Runsink J, Raabe G, Wendt B (2007b) Organocatalytic
one pot asymmetric synthesis of functionalized tricyclic carbon skeletons
via a triple cascade/Diels-Alder sequence. Angew Chem 119:471