Decoding the impact of solvents in altering the conversion rates and stereoselectivity in proline-catalyzed asymmetric aldol reaction

[1]  M. Lombardo,et al.  A Simple and Efficient Protocol for Proline-Catalysed Asymmetric Aldol Reaction , 2020, Catalysts.

[2]  Haiyang Zhang,et al.  Comparison of Implicit and Explicit Solvent Models for the Calculation of Solvation Free Energy in Organic Solvents. , 2017, Journal of chemical theory and computation.

[3]  Aniruddha Ghosh,et al.  Review of the aldol reaction , 2016 .

[4]  O. Lucchi,et al.  A Practical Synthesis of Rosuvastatin and Other Statin Intermediates , 2015 .

[5]  C. Dessent,et al.  Performance of M06, M06-2X, and M06-HF density functionals for conformationally flexible anionic clusters: M06 functionals perform better than B3LYP for a model system with dispersion and ionic hydrogen-bonding interactions. , 2013, The journal of physical chemistry. A.

[6]  Yahaya M. Normi,et al.  Various polar tripeptides as asymmetric organocatalyst in direct aldol reactions in aqueous media. , 2013, Chirality.

[7]  T. Kitanosono,et al.  Mukaiyama Aldol Reactions in Aqueous Media , 2013, Advanced synthesis & catalysis.

[8]  M. Murakami,et al.  The Mukaiyama aldol reaction: 40 years of continuous development. , 2013, Angewandte Chemie.

[9]  S. Kan,et al.  The impact of the Mukaiyama aldol reaction in total synthesis. , 2013, Angewandte Chemie.

[10]  Fangjun Xiong,et al.  Synthetic studies on statins. Part 1: a short and cyanide-free synthesis of atorvastatin calcium via an enantioselective aldol strategy , 2013 .

[11]  J. Młynarski,et al.  General switch in regioselectivity in the Mukaiyama aldol reaction of silyloxyfuran with aldehydes in aqueous solvents. , 2012, Chemical communications.

[12]  P. Ramachandran,et al.  Solvent- or temperature-controlled diastereoselective aldol reaction of methyl phenylacetate. , 2012, Organic letters.

[13]  Tian Lu,et al.  Multiwfn: A multifunctional wavefunction analyzer , 2012, J. Comput. Chem..

[14]  B. Trost,et al.  The direct catalytic asymmetric aldol reaction. , 2010, Chemical Society reviews.

[15]  A. Armstrong,et al.  A Coherent Mechanistic Rationale for Additive Effects and Autoinductive Behaviour in Proline-Mediated Reactions , 2009 .

[16]  Steven E. Wheeler,et al.  Accurate reaction enthalpies and sources of error in DFT thermochemistry for aldol, Mannich, and alpha-aminoxylation reactions. , 2009, The journal of physical chemistry. A.

[17]  P. Galletti,et al.  Evaluation of 6‐APA as a New Organocatalyst for a Direct Cross‐Aldol Reaction , 2009 .

[18]  P. G. Hultin,et al.  The state of the art in asymmetric induction: the aldol reaction as a case study , 2009 .

[19]  K. Nakayama,et al.  Complete switch of product selectivity in asymmetric direct aldol reaction with two different chiral organocatalysts from a common chiral source. , 2008, Journal of the American Chemical Society.

[20]  Edward G Hohenstein,et al.  Assessment of the Performance of the M05-2X and M06-2X Exchange-Correlation Functionals for Noncovalent Interactions in Biomolecules. , 2008, Journal of chemical theory and computation.

[21]  A. Armstrong,et al.  Clarification of the role of water in proline-mediated aldol reactions. , 2007, Journal of the American Chemical Society.

[22]  A. Fernández-Mayoralas,et al.  Asymmetric aldol reaction catalyzed by a heterogenized proline on a mesoporous support. The role of the nature of solvents. , 2007, The Journal of organic chemistry.

[23]  K. Janda,et al.  Enamine-based aldol organocatalysis in water: are they really "all wet"? , 2006, Angewandte Chemie.

[24]  M. Amedjkouh Primary amine catalyzed direct asymmetric aldol reaction assisted by water , 2005 .

[25]  R. Mestres A green look at the aldol reaction , 2004 .

[26]  L. Domingo,et al.  Density functional theory study of the mechanism of the proline-catalyzed intermolecular aldol reaction , 2002 .

[27]  James W. Gauld,et al.  Density Functional Study of the Proline-Catalyzed Direct Aldol Reaction , 2002 .

[28]  H. Shimizu,et al.  Highly anti-selective asymmetric aldol reactions using chiral zirconium catalysts. Improvement of activities, structure of the novel zirconium complexes, and effect of a small amount of water for the preparation of the catalysts. , 2002, Journal of the American Chemical Society.

[29]  K N Houk,et al.  Transition states of amine-catalyzed aldol reactions involving enamine intermediates: theoretical studies of mechanism, reactivity, and stereoselectivity. , 2001, Journal of the American Chemical Society.

[30]  C. Barbas,et al.  Amino acid catalyzed direct asymmetric aldol reactions: a bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reactions. , 2001, Journal of the American Chemical Society.

[31]  S. Nagayama,et al.  A Novel Chiral Lead(II) Catalyst for Enantioselective Aldol Reactions in Aqueous Media , 2000 .

[32]  F Zanardi,et al.  The vinylogous aldol reaction: a valuable, yet understated carbon-carbon bond-forming maneuver. , 2000, Chemical reviews.

[33]  Richard A. Lerner,et al.  Proline-Catalyzed Direct Asymmetric Aldol Reactions , 2000 .

[34]  C. Cramer,et al.  Implicit Solvation Models: Equilibria, Structure, Spectra, and Dynamics. , 1999, Chemical reviews.

[35]  K Schulten,et al.  VMD: visual molecular dynamics. , 1996, Journal of molecular graphics.