Max Knollmüller, Dr. techn.

Affiliations: 
Organic Chemistry TU Vienna 
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"Max Knollmüller"
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Noe CR, Knollmüller M, Jangg E, et al. (2009) Increasing chiral recognition in acetal formation. Chirality. 21: 428-35
Gärtner P, Novak C, Einzinger C, et al. (2003) A facile and high yielding synthesis of 2,2,3,4,4-d5-androsterone-beta-D-glucuronide--an internal standard in dope. Steroids. 68: 85-96
Gärtner P, Knollmüller M, Bröker J. (2003) Stereoselectivity in Pinacol-Homocoupling Mediated by Samarium Diiodide Monatshefte Fur Chemie. 134: 1607-1615
Gärtner P, Novak C, Knollmüller M, et al. (2001) Lithium tri-sec-butylborodeuteride: A new reagent for the stereoselective deuterium addition to cyclohexanones with single chair conformations Arkivoc. 2001: 9-20
Gärtner P, Letschnig MF, Knollmüller M, et al. (2000) [1,2]-Wittig rearrangement of acetals. Part 2: The influence of reaction conditions1 Tetrahedron Asymmetry. 11: 1003-1013
Gärtner P, Letschnig M, Knollmüller M. (2000) [1,2]-Wittig rearrangement of acetals iii [1]. New 1,2-alkoxyalcohols, 1,2-alkoxyamines and 1,2-dialkoxy compounds as chiral ligands for organomagnesium and organolithium compounds and for lithium aluminum hydride Monatshefte Fur Chemie. 131: 867-877
Gärtner P, Letschnig MF, Knollmüller M, et al. (1999) [1,2]-Wittig rearrangement of acetals. Part 1: Investigation about structural requirements Tetrahedron Asymmetry. 10: 4811-4830
Knollmüller M, Ferencic M, Gärtner P. (1999) Enantioselective addition of organometallics to aldehydes using camphor derived chiral 1,4-aminoalcohols as ligands Tetrahedron Asymmetry. 10: 3969-3975
Knollmüller M, Gärtner P, Pernerstorfer J, et al. (1999) Aminoalcohols V [1]: A method for the synthesis of enantiomerically pure ring-chlorinated epinephrines and norepinephrines Monatshefte Fur Chemie. 130: 451-470
Knollmüller M, Ferencic M, Gärtner P, et al. (1999) Addition of enantiomerically pure amines to activated olefines II. On the addition to ethyl (E)-4-oxo-4-phenyl-2-butenoate | Addition von enantiomerenreinen aminen an aktivierte olefine, 2. mitt. über die addition an (E)-4-oxo-4-phenyl-2-butensäure-ethylester Monatshefte Fur Chemie. 130: 769-782
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