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- Bioreduction of α-methylcinnamaldehyde derivatives: chemo-enzymatic asymmetric synthesis of Lilial™ and Helional™. Clemens Stueckler, Nicole J. Mueller, Christoph K. Winkler, Silvia M. Glueck, Karl Gruber, Georg Steinkellner, Kurt Faber
, Dalton Trans.
, 2010
, 39
, 8472
- Kinetic resolution of primary 2-methyl-substituted alcohols via
Pseudomonas cepacia lipase-catalysed enantioselective acylation. Ove Nordin, Ba-Vu Nguyen, Carin Vörde, Erik Hedenström, Hans-Erik Högberg
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 367
- Cyclometalated (NNC)Ru(ii) complex catalyzed β-methylation of alcohols using methanol. Kasturi Ganguli, Natalia V. Belkova, Sabuj Kundu
, Dalton Trans.
, 2022
, 51
, 4354
- A general approach for the asymmetric synthesis of densely substituted piperidines and fully substituted piperidinones employing the asymmetric Mannich reaction as key step. Ainara Iza, Uxue Uria, Efraím Reyes, Luisa Carrillo, Jose L. Vicario
, RSC Adv.
, 2013
, 3
, 25800
- SuperQuat N-acyl-5,5-dimethyloxazolidin-2-ones for the asymmetric synthesis of α-alkyl and β-alkyl aldehydes. Steven D. Bull, Stephen G. Davies, Rebecca L. Nicholson, Hitesh J. Sanganee, Andrew D. Smith
, Org. Biomol. Chem.
, 2003
, 1
, 2886
- Atropisomeric amides: stereoselective enolate chemistry and enantioselective synthesis via a new SmI2-mediated reduction. Adam D. Hughes, David A. Price, Nigel S. Simpkins
, J. Chem. Soc., Perkin Trans. 1
, 1999
, 1295
- A cleavable linker strategy for optimising enolate alkylation reactions of a polymer-supported Evans' oxazolidin-2-one. Rachel Green, Andrew T. Merritt, Steven D. Bull
, Chem. Commun.
, 2008
, 508
- Intramolecular mobility of η5-ligands in chiral zirconocene complexes and the enantioselectivity of alkene functionalization by organoaluminum compounds. Lyudmila V. Parfenova, Irina V. Zakirova, Pavel V. Kovyazin, Stanislav G. Karchevsky, Galina P. Istomina, Leonard M. Khalilov, Usein M. Dzhemilev
, Dalton Trans.
, 2016
, 45
, 12814
- The diastereoselectivity of electrophilic attack on trigonal carbon adjacent to a stereogenic centre: diastereoselective alkylation and protonation of open-chain enolates having a stereogenic centre carrying a silyl group at the β position. Roger A. N. C. Crump, Ian Fleming, John H. M. Hill, David Parker, N. Laxma Reddy, David Waterson
, J. Chem. Soc., Perkin Trans. 1
, 1992
, 3277
- Stereochemical course of the reduction of cinnamaldehyde and cinnamyl alcohol to 3-phenylpropanol by fermenting Baker's yeast. Claudio Fuganti, Dario Chiringhelli, Piero Grasselli
, J. Chem. Soc., Chem. Commun.
, 1975
, 846b