120
D. Enders, M.R.M. Hüttl, O. Niemeier
Okabe K, Keenan RW, Schmidt G (1968) Phytosphingosine groups as quantitatively significant components of the sphingolipids of the mucosa of the
small intestines of some mammalian species. Biochem Biophys Res Commun 31:137–143
Omar F, Frahm AW (1989) Asymmetrische reduktive Aminierung von Cycloalkanonen, 9. Mitt.: Die asymmetrische Synthese GABA-verwandter cycloaliphatischer Aminosäuren Arch Pharm 322:461
Omar F, Frahm AW (1990) Asymmetrische reduktive Aminierung von Cycloalkanonen, 10. Mitt.: EPC-Synthese cis-bicyclischer Lactame und
Amine. Arch Pharm 323:923
Pellisier H (2006) Asymmetric domino reactions. Part B: Reactions based on
the use of chiral catalysts and biocatalysts. Tetrahedron 62:2143
Pellissier H (2006) Asymmetric domino reactions. Part A: Reactions based on
the use of chiral auxiliaries. Tetrahedron 62:1619
Perry MC, Burgess K (2003) Chiral N-heterocyclic carbene-. transition metal
complexes in asymmetric catalysis. Tetrahedron Asymmetry 14:951–961
Piers E, Romero MA (1993) Total synthesis of amphilectane-type diterpenoids:
(±)-8-isocyano-10,14-amphilectadiene. Tetrahedron 49:5791
Pihko PM (2006) Enantioselective alpha-fluorination of carbonyl compounds:
organocatalysis or metal catalysis? Angew Chem Int Ed Engl 45:544–547
Prakash GK, Beier P (2006) Construction of asymmetric fluorinated carbon centers. Angew Chem Int Ed Engl 45:2172–2174
Prieto A, Halland N, Jørgensen KA (2005) Novel imidazolidine-tetrazole organocatalyst for asymmetric conjugate addition of nitroalkanes. Org Lett
7:3897–3900
Raabe G, Breuer K, Enders D (1996) The role of conjugate interaction in stable
carbenes of the 1,2,4-triazol-5-ylidene type and their energy of dimerisation. An ab initio study. Z Naturforsch [B] 51a:95–101
Ramón DJ, Yus M (2005) Asymmetric multicomponent reactions (AMCRs):
the new frontier. Angew Chem Int Ed Engl 44:1602–1634
Rassu G, Auzzas D, Pinna L, Battistini L, Zanardi F, Marzocchi L, Acquotti
D, Casiraghi G (2000) Variable strategy toward carbasugars and relatives.
1. Stereocontrolled synthesis of pseudo-beta-D-gulopyranose, pseudo-betaD-xylofuranose, (pseudo-beta-D-gulopyranosyl)amine, and (pseudo-betaD-xylofuranosyl)amine. J Org Chem 65:6307–6318
Read de Alaniz J, Rovis T (2005) A highly enantio- and diastereoselective catalytic intramolecular Stetter reaction. J Am Chem Soc 127:6284–6289
Reynolds NT, Rovis T (2005) The effect of pre-existing stereocenters in the
intramolecular asymmetric Stetter reaction. Tetrahedron 61:6368–6378
D. Enders, M.R.M. Hüttl, O. Niemeier
Okabe K, Keenan RW, Schmidt G (1968) Phytosphingosine groups as quantitatively significant components of the sphingolipids of the mucosa of the
small intestines of some mammalian species. Biochem Biophys Res Commun 31:137–143
Omar F, Frahm AW (1989) Asymmetrische reduktive Aminierung von Cycloalkanonen, 9. Mitt.: Die asymmetrische Synthese GABA-verwandter cycloaliphatischer Aminosäuren Arch Pharm 322:461
Omar F, Frahm AW (1990) Asymmetrische reduktive Aminierung von Cycloalkanonen, 10. Mitt.: EPC-Synthese cis-bicyclischer Lactame und
Amine. Arch Pharm 323:923
Pellisier H (2006) Asymmetric domino reactions. Part B: Reactions based on
the use of chiral catalysts and biocatalysts. Tetrahedron 62:2143
Pellissier H (2006) Asymmetric domino reactions. Part A: Reactions based on
the use of chiral auxiliaries. Tetrahedron 62:1619
Perry MC, Burgess K (2003) Chiral N-heterocyclic carbene-. transition metal
complexes in asymmetric catalysis. Tetrahedron Asymmetry 14:951–961
Piers E, Romero MA (1993) Total synthesis of amphilectane-type diterpenoids:
(±)-8-isocyano-10,14-amphilectadiene. Tetrahedron 49:5791
Pihko PM (2006) Enantioselective alpha-fluorination of carbonyl compounds:
organocatalysis or metal catalysis? Angew Chem Int Ed Engl 45:544–547
Prakash GK, Beier P (2006) Construction of asymmetric fluorinated carbon centers. Angew Chem Int Ed Engl 45:2172–2174
Prieto A, Halland N, Jørgensen KA (2005) Novel imidazolidine-tetrazole organocatalyst for asymmetric conjugate addition of nitroalkanes. Org Lett
7:3897–3900
Raabe G, Breuer K, Enders D (1996) The role of conjugate interaction in stable
carbenes of the 1,2,4-triazol-5-ylidene type and their energy of dimerisation. An ab initio study. Z Naturforsch [B] 51a:95–101
Ramón DJ, Yus M (2005) Asymmetric multicomponent reactions (AMCRs):
the new frontier. Angew Chem Int Ed Engl 44:1602–1634
Rassu G, Auzzas D, Pinna L, Battistini L, Zanardi F, Marzocchi L, Acquotti
D, Casiraghi G (2000) Variable strategy toward carbasugars and relatives.
1. Stereocontrolled synthesis of pseudo-beta-D-gulopyranose, pseudo-betaD-xylofuranose, (pseudo-beta-D-gulopyranosyl)amine, and (pseudo-betaD-xylofuranosyl)amine. J Org Chem 65:6307–6318
Read de Alaniz J, Rovis T (2005) A highly enantio- and diastereoselective catalytic intramolecular Stetter reaction. J Am Chem Soc 127:6284–6289
Reynolds NT, Rovis T (2005) The effect of pre-existing stereocenters in the
intramolecular asymmetric Stetter reaction. Tetrahedron 61:6368–6378