Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid ; day:07 ; month:02 ; year:2023 ; extent:7
Angewandte Chemie ; (07.02.2023) (gesamt 7)

Creator: Paczelt, Viktor
Wende, Raffael Christoph
Schreiner, Peter R.
Eckhardt, André K.

DOI: 10.1002/ange.202218548

URN: urn:nbn:de:101:1-2023020814032844063608

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:45 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Paczelt, Viktor
Wende, Raffael Christoph
Schreiner, Peter R.
Eckhardt, André K.

Other Objects (12)

Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid

Quantifying Reductive Amination in Nonenzymatic Amino Acid Synthesis

1,1‐Ethenediol: The Long Elusive Enol of Acetic Acid

Amino‐λ 3 ‐iodane‐Enabled Electrophilic Amination of Arylboronic Acid Derivatives

Hochschulschrift

Synthesis and characterization of novel poly(imino ketone)s via palladium-catalyzed aryl amination

Direct Synthesis of α‐Amino Acid Derivatives by Hydrative Amination of Alkynes

Systematic evaluation of imine‐reducing enzymes: common principles in imine reductases, [beta]‐hydroxy acid dehydrogenases, and short‐chain dehydrogenases/ reductases

Systematic Evaluation of Imine‐Reducing Enzymes: Common Principles in Imine Reductases, β‐Hydroxy Acid Dehydrogenases, and Short‐Chain Dehydrogenases/Reductases

Preparative Asymmetric Synthesis of Canonical and Non‐canonical α‐amino Acids Through Formal Enantioselective Biocatalytic Amination of Carboxylic Acids

Molybdenum‐Catalyzed Asymmetric Amination of α‐Hydroxy Esters: Synthesis of α‐Amino Acids

Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives †

Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid

Quantifying Reductive Amination in Nonenzymatic Amino Acid Synthesis

1,1‐Ethenediol: The Long Elusive Enol of Acetic Acid

Amino‐λ 3 ‐iodane‐Enabled Electrophilic Amination of Arylboronic Acid Derivatives

Hochschulschrift

Synthesis and characterization of novel poly(imino ketone)s via palladium-catalyzed aryl amination

Direct Synthesis of α‐Amino Acid Derivatives by Hydrative Amination of Alkynes

Systematic evaluation of imine‐reducing enzymes: common principles in imine reductases, [beta]‐hydroxy acid dehydrogenases, and short‐chain dehydrogenases/ reductases

Systematic Evaluation of Imine‐Reducing Enzymes: Common Principles in Imine Reductases, β‐Hydroxy Acid Dehydrogenases, and Short‐Chain Dehydrogenases/Reductases

Preparative Asymmetric Synthesis of Canonical and Non‐canonical α‐amino Acids Through Formal Enantioselective Biocatalytic Amination of Carboxylic Acids

Molybdenum‐Catalyzed Asymmetric Amination of α‐Hydroxy Esters: Synthesis of α‐Amino Acids

Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives †

Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid

Quantifying Reductive Amination in Nonenzymatic Amino Acid Synthesis

1,1‐Ethenediol: The Long Elusive Enol of Acetic Acid

Amino‐λ 3 ‐iodane‐Enabled Electrophilic Amination of Arylboronic Acid Derivatives

Hochschulschrift

Synthesis and characterization of novel poly(imino ketone)s via palladium-catalyzed aryl amination

Direct Synthesis of α‐Amino Acid Derivatives by Hydrative Amination of Alkynes

Systematic evaluation of imine‐reducing enzymes: common principles in imine reductases, [beta]‐hydroxy acid dehydrogenases, and short‐chain dehydrogenases/ reductases

Systematic Evaluation of Imine‐Reducing Enzymes: Common Principles in Imine Reductases, β‐Hydroxy Acid Dehydrogenases, and Short‐Chain Dehydrogenases/Reductases

Preparative Asymmetric Synthesis of Canonical and Non‐canonical α‐amino Acids Through Formal Enantioselective Biocatalytic Amination of Carboxylic Acids

Molybdenum‐Catalyzed Asymmetric Amination of α‐Hydroxy Esters: Synthesis of α‐Amino Acids

Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives †

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid

Quantifying Reductive Amination in Nonenzymatic Amino Acid Synthesis

1,1‐Ethenediol: The Long Elusive Enol of Acetic Acid

Amino‐λ 3 ‐iodane‐Enabled Electrophilic Amination of Arylboronic Acid Derivatives

Amino‐λ 3 ‐iodane‐Enabled Electrophilic Amination of Arylboronic Acid Derivatives

Synthesis and characterization of novel poly(imino ketone)s via palladium-catalyzed aryl amination

Direct Synthesis of α‐Amino Acid Derivatives by Hydrative Amination of Alkynes

Systematic evaluation of imine‐reducing enzymes: common principles in imine reductases, [beta]‐hydroxy acid dehydrogenases, and short‐chain dehydrogenases/ reductases

Systematic Evaluation of Imine‐Reducing Enzymes: Common Principles in Imine Reductases, β‐Hydroxy Acid Dehydrogenases, and Short‐Chain Dehydrogenases/Reductases

Preparative Asymmetric Synthesis of Canonical and Non‐canonical α‐amino Acids Through Formal Enantioselective Biocatalytic Amination of Carboxylic Acids

Molybdenum‐Catalyzed Asymmetric Amination of α‐Hydroxy Esters: Synthesis of α‐Amino Acids

Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives †

Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid

Quantifying Reductive Amination in Nonenzymatic Amino Acid Synthesis

1,1‐Ethenediol: The Long Elusive Enol of Acetic Acid

Amino‐λ 3 ‐iodane‐Enabled Electrophilic Amination of Arylboronic Acid Derivatives

Amino‐λ 3 ‐iodane‐Enabled Electrophilic Amination of Arylboronic Acid Derivatives

Synthesis and characterization of novel poly(imino ketone)s via palladium-catalyzed aryl amination

Direct Synthesis of α‐Amino Acid Derivatives by Hydrative Amination of Alkynes

Systematic evaluation of imine‐reducing enzymes: common principles in imine reductases, [beta]‐hydroxy acid dehydrogenases, and short‐chain dehydrogenases/ reductases

Systematic Evaluation of Imine‐Reducing Enzymes: Common Principles in Imine Reductases, β‐Hydroxy Acid Dehydrogenases, and Short‐Chain Dehydrogenases/Reductases

Preparative Asymmetric Synthesis of Canonical and Non‐canonical α‐amino Acids Through Formal Enantioselective Biocatalytic Amination of Carboxylic Acids

Molybdenum‐Catalyzed Asymmetric Amination of α‐Hydroxy Esters: Synthesis of α‐Amino Acids

Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives †

Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid

Quantifying Reductive Amination in Nonenzymatic Amino Acid Synthesis

1,1‐Ethenediol: The Long Elusive Enol of Acetic Acid

Amino‐λ 3 ‐iodane‐Enabled Electrophilic Amination of Arylboronic Acid Derivatives

Amino‐λ 3 ‐iodane‐Enabled Electrophilic Amination of Arylboronic Acid Derivatives

Synthesis and characterization of novel poly(imino ketone)s via palladium-catalyzed aryl amination

Direct Synthesis of α‐Amino Acid Derivatives by Hydrative Amination of Alkynes

Systematic evaluation of imine‐reducing enzymes: common principles in imine reductases, [beta]‐hydroxy acid dehydrogenases, and short‐chain dehydrogenases/ reductases

Systematic Evaluation of Imine‐Reducing Enzymes: Common Principles in Imine Reductases, β‐Hydroxy Acid Dehydrogenases, and Short‐Chain Dehydrogenases/Reductases

Preparative Asymmetric Synthesis of Canonical and Non‐canonical α‐amino Acids Through Formal Enantioselective Biocatalytic Amination of Carboxylic Acids

Molybdenum‐Catalyzed Asymmetric Amination of α‐Hydroxy Esters: Synthesis of α‐Amino Acids

Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives †

Related objects

Reset password