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Asymmetric Synthesis of β-Substituted α-Methyl-β-amino Esters by Mannich Reaction of (S,S)-(+)-Pseudoephedrine Acetamide Derived Enolate with Imines
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-3773(20000317)39:6<1063::aid-anie1063>3.0.co;2-yopenalex-snapshot
α-Oxymethyl Ketone Enolates for the Asymmetric Mannich Reaction. From Acetylene andN-Alkoxycarbonylimines toβ-Amino Acids
inferredcites →https://doi.org/10.1002/1521-3765(20000602)6:11<2032::aid-chem2032>3.0.co;2-bopenalex-snapshot
Asymmetric Steering of the Mannich Reaction with Phthaloyl Amino Acids
inferredcites →https://doi.org/10.1002/anie.199504331openalex-snapshot
Asymmetric Alkylation of Amide Enolates with Pseudoephedrine and Ephedrine as Chiral Auxiliaries—Unexpected Influence of Additives?
inferredcites →https://doi.org/10.1002/anie.199609811openalex-snapshot
Efficient Regio‐ and Enantioselective Mannich Reactions
inferredcites →https://doi.org/10.1002/anie.199703861openalex-snapshot
Asymmetric Mannich Synthesis of β‐Amino Acids with Two New Stereogenic Centers at the α and β Positions
inferredcites →https://doi.org/10.1016/0040-4020(95)00503-zopenalex-snapshot
Optically Active Aminoalcohol Promoted Addition of 2-Pyridylthioester Boron Enolates to Imines: Enantioselective One-pot Synthesis of β-Lactams
inferredcites →https://doi.org/10.1016/0040-4020(95)00997-3openalex-snapshot
Diastereofacial selectivity in the reaction of chiral N-trimethylsilyl imines with ester enolates: Preparation of trans-azetidin-2-ones in high stereocontrolled fashion.
inferredcites →https://doi.org/10.1016/0040-4039(94)02327-8openalex-snapshot
Creation of chirality in the reaction of the chiral ester enolate-imine condensation leading to the stereodivergent synthesis of β-lactams
inferredcites →https://doi.org/10.1016/0040-4039(95)00772-5openalex-snapshot
Asymmetric synthesis of trans and cis β-lactams
inferredcites →https://doi.org/10.1016/0040-4039(96)00108-6openalex-snapshot
Highly diastereoselective addition of silyl enolates to chiral imines derived from (S)-valine methyl ester using lanthanide triflate
inferredcites →https://doi.org/10.1016/0040-4039(96)00707-1openalex-snapshot
Switchover of diastereofacial selectivity in the condensation reaction of optically active N-sulfinimine with ester enolate
inferredcites →https://doi.org/10.1016/s0040-4020(01)88276-4openalex-snapshot
Syntheses of 3-amino-2-azetidinones: A literature survey
inferredcites →https://doi.org/10.1016/s0040-4020(97)00435-3openalex-snapshot
Computational studies on the aldol-type addition of boron enolates to imines: An ab-initio approach
inferredcites →https://doi.org/10.1016/s0040-4039(00)73085-1openalex-snapshot
First synthesis of optically pure α-amino amine as asymmetric amino transfer reagent and its use in asymmetric Mannich reaction
inferredcites →https://doi.org/10.1016/s0040-4039(00)78889-7openalex-snapshot
Stereoselective ring opening of chiral oxazolidines by reformatsky reagents: an enantioselective entry to β-amino esters.
inferredcites →https://doi.org/10.1016/s0040-4039(00)82286-8openalex-snapshot
New chiral recognition of chiral tin(II) enolates toward cyclic acyl iminium species. Asymmetric total synthesis of (−)-supinidine
inferredcites →https://doi.org/10.1016/s0040-4039(00)91831-8openalex-snapshot
Stereoselective synthesis of β-lactams by condensation of titanium enolates of 2-pyridylthioesters with imines bearing a chiral auxiliary
inferredcites →https://doi.org/10.1016/s0040-4039(00)92366-9openalex-snapshot
Highly enantioselective and diastereoselective synthesis of β-amino acid esters and β-lactams from achiral esters and imines
inferredcites →https://doi.org/10.1016/s0040-4039(00)95693-4openalex-snapshot
Asymmetric synthesis of trans- β -lactams through TiCl4-mediated addition to imines.
inferredcites →https://doi.org/10.1016/s0040-4039(00)96501-8openalex-snapshot
Diastereoselection in trimethylsilyl trifluoromethanesulphonatecatalyzed reaction of silyl ketene acetals with imines
inferredcites →https://doi.org/10.1016/s0040-4039(01)93810-9openalex-snapshot
Asymmetric alkylation of N-acylsultams: A general route to enantiomerically pure, crystalline C(α,α)-disubstituted carboxylic acid derivatives
inferredcites →https://doi.org/10.1016/s0040-4039(97)00130-5openalex-snapshot
Pyrrolidinopiperazinedione as chiral auxiliary and its use in asymmetric Mannich synthesis
inferredcites →https://doi.org/10.1016/s0040-4039(97)00963-5openalex-snapshot
Highly diastereoselective aza-aldol reactions of a chiral Ni(II) complex of glycine with imines. An efficient asymmetric approach to 3-perfluoroalkyl-2,3-diamino acids
inferredcites →https://doi.org/10.1016/s0040-4039(99)01475-6openalex-snapshot
Asymmetric synthesis of arylglycine amino acids using (S,S)-(+)-pseudoephedrine derived amides
inferredcites →https://doi.org/10.1016/s0957-4166(00)00343-8openalex-snapshot
Stereocontrolled metalloenamine alkylations: application to the asymmetric synthesis of 4-alkyl-1,2,3,4-tetrahydroisoquinolines
inferredcites →https://doi.org/10.1016/s0957-4166(99)00167-6openalex-snapshot
The first stereocontrolled synthesis of 12-methyl-hexahydrobenzo[c]phenanthridine alkaloids
inferredcites →https://doi.org/10.1021/cr980414zopenalex-snapshot
Catalytic Enantioselective Addition to Imines
inferredcites →https://doi.org/10.1021/ja00102a019openalex-snapshot
A New Chiral BLA Promoter for Asymmetric Aza Diels-Alder and Aldol-Type Reactions of Imines
inferredcites →https://doi.org/10.1021/ja00314a042openalex-snapshot
Unprecedented asymmetric induction from a chiral acetate enolate equivalent. The condensation of acetyl(triphenylphosphine)carbonyl-.eta.-cyclopentadienyliron [(.eta.-C5H5)Fe(CO)(PPh3)(Ac)] with imines
inferredcites →https://doi.org/10.1021/ja00329a029openalex-snapshot
N-Trimethylsilylimines: applications to the syntheses of .beta.-lactams
inferredcites →https://doi.org/10.1021/ja00987a030openalex-snapshot
Equilibrium in formation and conformational isomerization of imines derived from isobutyraldehyde and saturated aliphatic primary amines
inferredcites →https://doi.org/10.1021/ja01565a041openalex-snapshot
The Stereochemistry of the Ivanov and Reformatsky Reactions. I
inferredcites →https://doi.org/10.1021/ja963581uopenalex-snapshot
A Ternary Complex Reagent for an Asymmetric Reaction of Lithium Ester Enolates with Imines
inferredcites →https://doi.org/10.1021/ja970402fopenalex-snapshot
Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones
inferredcites →https://doi.org/10.1021/jo000035hopenalex-snapshot
Asymmetric Aldol Reactions Using (S,S)-(+)-Pseudoephedrine-Based Amides: Stereoselective Synthesis of α-Methyl-β-hydroxy Acids, Esters, Ketones, and 1,3-Syn and 1,3-Anti Diols
inferredcites →https://doi.org/10.1021/jo00005a048openalex-snapshot
Preparation of 3-amino-4-(hydroxymethyl)azetidin-2-ones from the reaction of glycine enolates with imines of a glycoaldehyde
inferredcites →https://doi.org/10.1021/jo00050a007openalex-snapshot
Asymmetric synthesis of sulfinimines: applications to the synthesis of nonracemic .beta.-amino acids and .alpha.-hydroxyl .beta.-amino acids
inferredcites →https://doi.org/10.1021/jo00119a009openalex-snapshot
Asymmetric Synthesis of .beta.-Lactams via the Zinc-Mediated Glycine Ester Enolate-Imine Condensation Reaction Using .alpha.-Amino Esters as the Chiral Auxiliary
inferredcites →https://doi.org/10.1021/jo01305a008openalex-snapshot
Preparation of .beta.-lactams by the condensation of lithium ester enolates with aryl aldimines
inferredcites →https://doi.org/10.1021/jo9708102openalex-snapshot
A Simple and Efficient Synthetic Route to Chiral Isopavines. Synthesis of (−)-O-Methylthalisopavine and (−)-Amurensinine
inferredcites →https://doi.org/10.1021/jo981326hopenalex-snapshot
Chiral Amino Alcohols As Intermediates in the Stereocontrolled Synthesis of 1,3-Disubstituted Tetrahydroisoquinolines and Protoberberines
inferredcites →https://doi.org/10.1021/jo982008lopenalex-snapshot
A New General Method for the Asymmetric Synthesis of 4-Alkyl-3-aryl-1,2,3,4-tetrahydroisoquinolines
inferredcites →https://doi.org/10.1021/jo982059iopenalex-snapshot
Synthesis of Enantiomerically Pure N-tert-Butanesulfinyl Imines (tert-Butanesulfinimines) by the Direct Condensation of tert-Butanesulfinamide with Aldehydes and Ketones
inferredcites →https://doi.org/10.1021/jo9822481openalex-snapshot
(3R)-Chiral Control of 3-Alkyl-3-hydroxy-β-lactams via Addition Reaction of Imines to Enolates of 1,3-Dioxolan-4-ones
inferredcites →https://doi.org/10.1021/jo990913fopenalex-snapshot
Lewis Acid Mediated Addition of Silyl Ketene Acetals to Sulfinimines
inferredcites →https://doi.org/10.1021/jo9909397openalex-snapshot
Stereoselective Mannich-Type Reaction of an Acyclic Ketimine with a Substituted Chlorotitanium Enolate: Efficient Approach to d -erythro-α-Trifluoromethylβ-hydroxyaspartic Units
inferredcites →https://doi.org/10.1021/ol9905755openalex-snapshot
Asymmetric Synthesis of β-Amino Acids by Addition of Chiral Enolates to N-Acyloxyiminium Ions and Application for Synthesis of Optically Active 5-Substituted 8-Methylindolizidines
inferredcites →https://doi.org/10.1055/s-1998-1718openalex-snapshot
Diastereoselective Addition of Silyl Enol Ether to Chiral Imines and 1,3-Oxazolidines Using a Lewis Acid
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Stereoselective Alkylation of Imines and its Application towards the Synthesis of β‐Lactams
inferred← citeshttps://doi.org/10.1002/ange.200350890openalex-snapshot
Vanadium‐Catalyzed anti‐Selective Additions of Allenols to Imines
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Vanadium‐Catalyzed anti‐Selective Additions of Allenols to Imines
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The Direct Catalytic Asymmetric Cross‐Mannich Reaction: A Highly Enantioselective Route to 3‐Amino Alcohols and α‐Amino Acid Derivatives
inferred← citeshttps://doi.org/10.1002/chin.200127069openalex-snapshot
ChemInform Abstract: Asymmetric Synthesis of β‐Substituted α‐Methyl‐β‐amino Esters by Mannich Reaction of (S,S)‐(+)‐Pseudoephedrine Acetamide Derived Enolate with Imines.
inferred← citeshttps://doi.org/10.1016/b978-0-12-417034-6.00010-4openalex-snapshot
Addition To C=N Bonds
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00306-0openalex-snapshot
Furans and their Benzo Derivatives: Reactivity
inferred← citeshttps://doi.org/10.1016/j.tet.2003.11.012openalex-snapshot
LiClO4 Accelerated Michael addition of amines to α,β-unsaturated olefins under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2015.01.060openalex-snapshot
Recent advances in the stereoselective syntheses of acyclic disubstituted β2,3-amino acids
inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.09.006openalex-snapshot
Asymmetric and diastereoselective Mannich reactions using hydantoin as a chiral auxiliary
inferred← citeshttps://doi.org/10.1016/j.tetasy.2014.11.008openalex-snapshot
Investigation of the diastereoselective Mannich reaction using imidazolidin-2-thione as a chiral auxiliary
inferred← citeshttps://doi.org/10.1016/s0040-4020(02)00991-2openalex-snapshot
Recent advances in the stereoselective synthesis of β-amino acids
inferred← citeshttps://doi.org/10.1016/s0957-4166(02)00260-4openalex-snapshot
Stereoselective Mannich reaction of camphor titanium enolate
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A new protocol for the one-pot preparation of highly diastereomerically enriched secondary amines and β-amino esters mediated by lithium perchlorate solution in diethyl ether
inferred← citeshttps://doi.org/10.1016/s0957-4166(02)00831-5openalex-snapshot
An easy and straightforward approach to the asymmetric synthesis of isoflavanones
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Mannich-Type Reaction of α-Sulfanyl N - tert -Butanesulfinylimidates: Diastereoselective Access to α-Mercapto-β-amino Acid Derivatives
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Stereocontrolled Mannich Reaction with Enolizable Imines Using (S,S)-(+)-Pseudoephedrine as Chiral Auxiliary. Asymmetric Synthesis of α,β-Disubstituted β-Aminoesters and β-Lactams
inferred← citeshttps://doi.org/10.1021/jo035564aopenalex-snapshot
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(S,S)-(+)-Pseudoephedrine as Chiral Auxiliary in Asymmetric Conjugate Addition and Tandem Conjugate Addition/α-Alkylation Reactions
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