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References from Highly Catalytic Enantioselective Reformatsky Reaction with Aldehydes and Ketones Using an Available Prolinol Ligand. Local targets link to admitted publications; unresolved targets remain external evidence.
Neue Synthese zweiatomiger einbasischer Säuren aus den Ketonen
10.1002/cber.188702001268 · 1887 · External reference
The Reformatsky reaction in organic synthesis. Recent advances
10.1016/j.tet.2004.07.018 · 2004 · External reference
In- or In(I)-employed tailoring of the stereogenic centers in the Reformatsky-type reactions of simple ketones, α-alkoxy ketones, and β-keto esters
10.1021/jo051659w · 2005 · External reference
Recent advancements in the Reformatsky reaction
10.1055/s-1989-27326 · 1989 · External reference
10.1093/oso/9780198501213.003.0019
10.1093/oso/9780198501213.003.0019 · 1999 · External reference
Rhodium-catalyzed Reformatskii reaction
2000 · External reference
Indium in organic synthesis
10.1055/s-2003-38064 · 2003 · External reference
Transition metals-mediated Reformatsky reactions
10.2174/1570179043485385 · 2004 · External reference
Unresolved reference
2002 · External reference
Reformatsky and Blaise reactions in flow as a tool for drug discovery. One pot diversity oriented synthesis of valuable intermediates and heterocycles
10.1039/c6gc02619b · 2017 · External reference
An improved asymmetric Reformatsky reaction mediated by (−)-N, N-dimethylaminoisoborneol
10.1021/ol0531381 · 2006 · External reference
Remote stereoinduction in the acylation of fully substituted enolates: tandem Reformatsky/quaternary Claisen condensations of silyl glyoxylates and β-lactones
10.1021/ja108848d · 2010 · External reference
Recent Advances in the Catalytic Enantioselective Reformatsky Reaction
10.1002/ejoc.201300571 · 2013 · External reference
Recent developments in the asymmetric Reformatsky-type reaction
10.3762/bjoc.14.21 · 2018 · External reference
Synthesis of α-fluoro-β-hydroxy esters by an enantioselective Reformatsky-type reaction
10.1039/c2cc17985g · 2012 · External reference
A Catalytic, Me2Z-mediated, enantioselective Reformatsky reaction with ketones
10.1002/anie.200504239 · 2006 · External reference
Rhodium-catalyzed Reformatsky-type reaction
10.1021/ol006268c · 2000 · External reference
A simple and efficient procedure of low valent iron-or copper-mediated reformatsky reaction of aldehydes
10.1021/jo0710984 · 2007 · External reference
The Reformatsky reaction. I. Condensation of ketones and t-butyl bromoacetate by magnesium
10.1021/jo01341a524 · 1966 · External reference
Manganese ate complexes as new reducing agents: Perfectly regiocontrolled generation and reactions of the manganese enolates with electrophiles
10.1021/ja964054d · 1997 · External reference
Synthesis of β-hydroxy esters using highly active manganese
10.1016/j.tetlet.2003.11.045 · 2004 · External reference
Iron-catalysed reformatsky-type reactions
10.1055/s-2006-926432 · 2006 · External reference
Reformatsky reactions with SmI2 in catalytic amount
10.1016/j.tetlet.2005.01.079 · 2005 · External reference
A short stereoselective synthesis of prepiscibactin using a SmI2-mediated Reformatsky reaction and Zn2+-induced asymmetric thiazolidine formation
10.1021/ol502958u · 2014 · External reference
Samarium iodide-mediated reformatsky reactions for the stereoselective preparation of β-hydroxy-γ-amino acids: synthesis of isostatine and dolaisoleucine
10.1021/jo202091r · 2012 · External reference
Chromium (II)-mediated Reformatsky reactions of carboxylic esters with aldehydes
10.1021/jo961910v · 1997 · External reference
The direct preparation of organocadmium compounds from highly reactive cadmium metal powders
10.1021/jo00203a036 · 1985 · External reference
An activated Germanium metal-promoted, highly diastereoselective Reformatsky reaction
10.1021/jo971672j · 1998 · External reference
Carbon-carbon bond-forming reactions using cerium metal or organocerium (III) reagents
10.1021/jo00195a006 · 1984 · External reference
Activated metals. IX. New reformatsky reagent involving activated indium for the preparation of beta-hydroxy esters
10.1021/jo00903a031 · 1975 · External reference
In- or In (I)-employed diastereoselective Reformatsky-type reactions with ketones: 1H NMR investigations on the active species
10.1021/ol0482846 · 2004 · External reference
Total synthesis of (−)-dihydrosporothriolide utilizing an Indium-mediated Reformatsky–Claisen rearrangement
10.1021/jo5008948 · 2014 · External reference
Indium-promoted Reformatsky reaction: a straightforward access to β-amino and β-hydroxy α, α-difluoro carbonyl compounds
10.1021/jo301873y · 2012 · External reference
Iron (0)-mediated Reformatsky reaction for the synthesis of β-hydroxyl carbonyl compounds
10.1021/acs.orglett.9b01999 · 2019 · External reference
Me2Zn mediated, tert-butylhydroperoxide promoted, catalytic enantioselective Reformatsky reaction with aldehydes
10.1039/b805197f · 2008 · External reference
Dimethylzinc-mediated, oxidatively promoted Reformatsky reaction of ethyl iodoacetate with aldehydes and ketones
10.1002/adsc.200700572 · 2008 · External reference
Copper-promoted enantioselective Reformatsky-type reaction with ketones
10.1016/j.tetasy.2010.04.058 · 2010 · External reference
A catalytic, Me2Zn-mediated, enantioselective Reformatsky reaction with ketones
10.1002/anie.200504239 · 2006 · External reference
Practical chloromanganese–salen-catalyzed enantioselective Reformatsky reaction with ketones
10.1055/s-2007-983780 · 2007 · External reference
Catalytic enantioselective Reformatsky reaction with aldehydes
10.1002/anie.200704841 · 2008 · External reference
Catalytic enantioselective Reformatsky reaction with ketones
10.1039/b801749b · 2008 · External reference
Catalytic enantioselective Reformatsky reaction with ortho-substituted diarylketones
10.1021/ol801574m · 2008 · External reference
Bisoxazolidine-catalyzed enantioselective Reformatsky reaction
10.1021/jo200774e · 2011 · External reference
Catalytic enantioselective Reformatsky reaction of alkyl iodoacetate with aldehydes catalyzed by chiral Schiff base
10.1246/cl.2008.1298 · 2008 · External reference
Highly efficient asymmetric Michael reaction of aldehydes to nitroalkenes with diphenylperhydroindolinol silyl ethers as organocatalysts
10.1002/adsc.200900355 · 2009 · External reference
Indolinylmethanol catalyzed enantioselective Reformatsky reaction with ketones
10.1016/j.tetasy.2010.11.004 · 2010 · External reference
Catalytic enantioselective aza-Reformatsky reaction with cyclic imines
10.1002/chem.201604606 · 2016 · External reference
Catalytic enantioselective aza-Reformatsky reaction with seven-membered cyclic imines dibenzo[b,f][1,4]oxazepines
10.1039/c7qo00329c · 2017 · External reference
A new chemoenzymatic enantioselective synthesis of R-(−)-tomoxetine, (R)- and (S)-fluoxetine
10.1016/s0040-4039(00)85993-6 · 1991 · External reference
Asymmetric deprotonations: lithiation of N-(tert-butoxycarbonyl)indoline with sec-butyllithium/(−)-Sparteine
10.1021/jo9708856 · 1997 · External reference
