118
D. Enders, M.R.M. Hüttl, O. Niemeier
Marigo M, Fielenbach D, Braunton A, Kjoersgaard A, Jørgensen KA (2005a)
Enantioselective formation of stereogenic carbon-fluorine centers by a simple catalytic method. Angew Chem 117:3769
Marigo M, Schulte T, Franzén J, Jørgensen KA (2005b) Asymmetric multicomponent domino reactions and highly enantioselective conjugated addition of
thiols to alpha,beta-unsaturated aldehydes. J Am Chem Soc
127:15710–15711
Matsumoto T, Inoue S (1983) Selective formation of triose from formaldehyde
catalysed by ethylbenzothiazolium bromide. J Chem Soc Chem Commun
1983:171–172
Matsumoto T, Yamamoto H, Inoue S (1984) Selective formation of triose from
formaldehyde catalyzed by thiazolium salt. J Am Chem Soc 106:4829
Mattson AE, Bharadwaj AR, Scheidt KA (2004) The thiazolium-catalyzed SilaStetter reaction: conjugate addition of acylsilanes to unsaturated esters and
ketones. J Am Chem Soc 126:2314–2315
Mattson AE, Bharadwaj AR, Zuhl AM, Scheidt KA (2006a) Thiazolium-catalyzed additions of acylsilanes: a general strategy for acyl anion addition
reactions. J Org Chem 71:5715–5724
Mattson AE, Zuhl AM, Reynolds TE, Scheidt KA (2006b) Direct nucleophilic
acylation of nitroalkenes promoted by a fluoride anion/thiourea combination. J Am Chem Soc 128:4932–4933
McCasland GE, Furuta S, Durham LJ (1966) Alicyclic carbohydrates. XXIX.
The synthesis of a pseudo-hexose (2,3,4,5-tetrahydroxycyclohexanemethanol). J Org Chem 31:1516
Mehta G, Lakshminath S (2000) A norbornyl route to cyclohexitols: stereoselective synthesis of conduritol-E, allo-inositol, MK 7607 and gabosines.
Tetrahedron Lett 41:3509
Mennen MS, Gipson JD, Kim YR, Miller SJ (2005a) Thiazolylalanine-derived
catalysts for enantioselective intermolecular aldehyde-imine cross-couplings. J Am Chem Soc 127:1654
Mennen SM, Blank JT, Tran-Dubé MB, Imbriglio JE, Miller SJ (2005b) A peptide-catalyzed asymmetric Stetter reaction. Chem Commun 2005:195–197
Mizuhara S, Tamura R, Arata H (1951) The mechanism of thiamine action II.
Proc Jpn Acad 27:302
Moore JL, Kerr MS, Rovis T (2006) Enantioselective formation of quaternary
stereocenters using the catalytic intramolecular Stetter reaction. Tetrahedron 62:11477–11482
Mukaiyama T, Suzuki K, Yamada T, Tabusa F (1990) 4-O-Benzyl-23-O-isopropylidene-L-threose: a useful building block for stereoselective synthesis of
monosaccharides. Tetrahedron 46:265
D. Enders, M.R.M. Hüttl, O. Niemeier
Marigo M, Fielenbach D, Braunton A, Kjoersgaard A, Jørgensen KA (2005a)
Enantioselective formation of stereogenic carbon-fluorine centers by a simple catalytic method. Angew Chem 117:3769
Marigo M, Schulte T, Franzén J, Jørgensen KA (2005b) Asymmetric multicomponent domino reactions and highly enantioselective conjugated addition of
thiols to alpha,beta-unsaturated aldehydes. J Am Chem Soc
127:15710–15711
Matsumoto T, Inoue S (1983) Selective formation of triose from formaldehyde
catalysed by ethylbenzothiazolium bromide. J Chem Soc Chem Commun
1983:171–172
Matsumoto T, Yamamoto H, Inoue S (1984) Selective formation of triose from
formaldehyde catalyzed by thiazolium salt. J Am Chem Soc 106:4829
Mattson AE, Bharadwaj AR, Scheidt KA (2004) The thiazolium-catalyzed SilaStetter reaction: conjugate addition of acylsilanes to unsaturated esters and
ketones. J Am Chem Soc 126:2314–2315
Mattson AE, Bharadwaj AR, Zuhl AM, Scheidt KA (2006a) Thiazolium-catalyzed additions of acylsilanes: a general strategy for acyl anion addition
reactions. J Org Chem 71:5715–5724
Mattson AE, Zuhl AM, Reynolds TE, Scheidt KA (2006b) Direct nucleophilic
acylation of nitroalkenes promoted by a fluoride anion/thiourea combination. J Am Chem Soc 128:4932–4933
McCasland GE, Furuta S, Durham LJ (1966) Alicyclic carbohydrates. XXIX.
The synthesis of a pseudo-hexose (2,3,4,5-tetrahydroxycyclohexanemethanol). J Org Chem 31:1516
Mehta G, Lakshminath S (2000) A norbornyl route to cyclohexitols: stereoselective synthesis of conduritol-E, allo-inositol, MK 7607 and gabosines.
Tetrahedron Lett 41:3509
Mennen MS, Gipson JD, Kim YR, Miller SJ (2005a) Thiazolylalanine-derived
catalysts for enantioselective intermolecular aldehyde-imine cross-couplings. J Am Chem Soc 127:1654
Mennen SM, Blank JT, Tran-Dubé MB, Imbriglio JE, Miller SJ (2005b) A peptide-catalyzed asymmetric Stetter reaction. Chem Commun 2005:195–197
Mizuhara S, Tamura R, Arata H (1951) The mechanism of thiamine action II.
Proc Jpn Acad 27:302
Moore JL, Kerr MS, Rovis T (2006) Enantioselective formation of quaternary
stereocenters using the catalytic intramolecular Stetter reaction. Tetrahedron 62:11477–11482
Mukaiyama T, Suzuki K, Yamada T, Tabusa F (1990) 4-O-Benzyl-23-O-isopropylidene-L-threose: a useful building block for stereoselective synthesis of
monosaccharides. Tetrahedron 46:265