A unique approach to aldol products for the creation of all-carbon quaternary stereocentres

References

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	Year	Citations
Catalytic Enantioselective Construction of All-Carbon Quaternary Stereocenters Barry M. Trost, Chunhui Jiang Synthesis Chemical EngineeringEngineeringNatural SciencesDiversity-oriented SynthesisOrganic Chemistry	2006	983
Stereoselective Construction of Quaternary Stereocenters Jens Christoffers, Angelika Baro Advanced Synthesis & Catalysis Geometric ModelingOptical MaterialsAbstract Quaternary StereocentersEngineeringGeometry	2005	515
Carbometallation (<i>C</i>-Metallation) of Alkynes: Stereospecific Synthesis of Alkenyl Derivatives J. F. NORMANT, Alexandre Alexakis Synthesis Organic ChemistryAlkenyl DerivativesStereoselective SynthesisChemistry	1981	484
Synthesis of β‐Hydroxyaldehydes with Stereogenic Quaternary Carbon Centers by Direct Organocatalytic Asymmetric Aldol Reactions Nobuyuki Mase, Fujie Tanaka, Carlos F. Barbas Angewandte Chemie International Edition Catalyst SystemNovel OrganocatalystsEnantioselective SynthesisEngineeringNatural Sciences	2004	247
Creation of quaternary stereocenters in carbonyl allylation reactions Ilan Marek, Genia Sklute Chemical Communications Cross-coupling ReactionEngineeringPowerful ApproachesQuaternary StereocentersOrganic Chemistry	2006	230
A Copper-Catalyzed C−N Bond Formation Involving sp-Hybridized Carbons. A Direct Entry to Chiral Ynamides via N-Alkynylation of Amides Michael O. Frederick, Jason A. Mulder, Richard P. Hsung, Journal of the American Chemical Society	2003	226
A Copper‐Catalyzed C—N Bond Formation Involving sp‐Hybridized Carbons. Direct Entry to Chiral Ynamides via N‐Alkynylation of Amides. Michael O. Frederick, Jason A. Mulder, M. R. Tracey, ChemInform	2003	184
Selective mono- and polymethylene homologations of copper reagents using (iodomethyl)zinc iodide Achyutharao Sidduri, Michael J. Rozema, Paul Knochel The Journal of Organic Chemistry Materials ScienceChemical EngineeringEngineeringCopper ReagentsChemical Analysis	1993	118
Regio- and diastereoselective preparation of aldols from .alpha.-branched ketone enolates generated from BHT ester enolates and organolithium reagents. In situ generation and trapping of ketenes from ester enolates R. HAENER, Thomas Laube, Dieter Seebàch Journal of the American Chemical Society .Alpha.-branched Ketone EnolatesEngineeringBiochemistryAltmetric Attention ScoreOrganic Chemistry	1985	105
Acyclic Stereocontrol in the Ireland–Claisen Rearrangement of α‐Branched Esters Ying‐Chuan Qin, Craig E. Stivala, Armen Zakarian Angewandte Chemie International Edition Chiral AmidesPoor DiastereoselectivityEngineeringIreland–claisen RearrangementNatural Sciences	2007	105

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