Negishi cross-couplings in the synthesis of amino acids

Literature Information

Publication Date 2017-11-27
DOI 10.1039/C7OB02682J
Impact Factor 3.876
Authors

William D. G. Brittain, Steven L. Cobb


View Original

Abstract

The Negishi cross-coupling is a powerful C–C bond-forming reaction widely utilised in many areas of organic synthesis. This review details the use of Negishi cross-couplings in the synthesis of unnatural amino acids. The application of this reaction in the preparation of aromatic, heteroaromatic, and, complex amino acid derivatives are reviewed and presented herein.

Related Literature

Recyclable and efficient polyurethane-Ir catalysts for direct borylation of aromatic compounds

Akihiro Kimura, Haruka Hayama, Hassan Nageh, Yue Wang, Naofumi Naga

2017-11-09 Paper

DOI: 10.1039/C7PY01509G

Self-assembly and multi-stimuli responsive behavior of PAA-b-PAzoMA-b-PNIPAM triblock copolymers

Fei Gao, Yaohui Xing, Yuan Yao, Liuying Sun, Yao Sun, Xiaohua He, Shaoliang Lin

2017-10-31 Paper

DOI: 10.1039/C7PY01591G

CuAAC click chemistry: a versatile approach towards PVDF-based block copolymers

I. Terzic, N. L. Meereboer, K. Loos

2018-06-25 Communication

DOI: 10.1039/C8PY00742J

A new echelon of precision polypentenamers: highly isotactic branching on every five carbons

Stefan Brits, William J. Neary, Goutam Palui, Justin G. Kennemur

2018-01-02 Paper

DOI: 10.1039/C7PY01922J

Photopolymerization processes of thick films and in shadow areas: a review for the access to composites

Patxi Garra, Céline Dietlin, Fabrice Morlet-Savary, Frédéric Dumur, Didier Gigmes, Jean-Pierre Fouassier, Jacques Lalevée

2017-11-08 Review Article

DOI: 10.1039/C7PY01778B

Front cover

Cover

DOI: 10.1039/C8PY90018C

Reversible star assembly of polyolefins using interconversion between boroxine and boronic acid

Ryo Tanaka, Naoki Tonoko, Shin-ichi Kihara, Yuushou Nakayama, Takeshi Shiono

2018-06-12 Paper

DOI: 10.1039/C8PY00519B

Continuous-flow chemistry for the determination of comonomer reactivity ratios

Marcus H. Reis, Cullen L. G. Davidson, IV, Frank A. Leibfarth

2018-01-05 Paper

DOI: 10.1039/C7PY01938F

Visible light-induced iniferter polymerization of methacrylates enhanced by continuous flow

Maarten Rubens, Phanumat Latsrisaeng

2017-08-16 Paper

DOI: 10.1039/C7PY01157A

You might also like

Compound Q&A

What are the main uses of (3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8)?

(3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8) is primari...

79066-03-8(3.beta.)-3-Hydroxy-...
Compound Q&A

What regulatory guidelines apply to 5-(aminomethyl)-2-methoxyphenol (CAS: 89702-89-6)?

5-(Aminomethyl)-2-methoxyphenol (CAS: 89702-89-6) is classified under GHS as a s...

89702-89-65-(aminomethyl)-2-me...
Compound Q&A

What is Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7)?

Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7) is a heterocyclic organic compo...

28981-13-7Thieno[2,3-c]pyridin...
Compound Q&A

Is 1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride (CAS: 1185311-28-7) safe?

1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride is generally ...

1185311-28-71-[(6-Methoxy-3-pyri...
Compound Q&A

What regulatory guidelines apply to [(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2)?

[(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2) is regulated und...

146404-58-2[(2E)-3-Phenyl-2-pro...
Compound Q&A

What regulatory guidelines apply to 6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7)?

6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7) falls under the scope of the Glob...

1620515-86-76-Bromo-7-methoxyqui...
Compound Q&A

What industries use (2R)-1-(1-Benzofuran-2-yl)-N-propyl-2-pentanamine (CAS: 260550-89-8)?

This compound is primarily used in the pharmaceutical industry for the developme...

260550-89-8(2R)-1-(1-Benzofuran...
1228013-15-71-Ethyl-7-[2-methyl-...
Compound Q&A

Are there alternatives to {5-(Acryloylamino)-2-[(dimethylamino)methyl]phenyl}boronic acid (CAS: 1217500-78-1) in synthesis?

Alternative reagents such as 2-[(dimethylamino)methyl]phenylboronic acid or rela...

1217500-78-1{5-(Acryloylamino)-2...
Compound Q&A

What is 3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2)?

3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2) is an organic compound with the...

310881-48-23-(Piperidin-4-yloxy...

Source Journal

Organic & Biomolecular Chemistry

Organic & Biomolecular Chemistry
CiteScore: 3.4
Self-citation Rate: 10.3%
Articles per Year: 1041

Organic & Biomolecular Chemistry (OBC) publishes original and high impact research and reviews in organic chemistry. We welcome research that shows new or significantly improved protocols or methodologies in total synthesis, synthetic methodology or physical and theoretical organic chemistry as well as research that shows a significant advance in the organic chemistry or molecular design aspects of chemical biology, catalysis, supramolecular and macromolecular chemistry, theoretical chemistry, mechanism-oriented physical organic chemistry, medicinal chemistry or natural products. Articles published in the journal should report new work which makes a highly-significant impact in the field. Routine and incremental work is generally not suitable for publication in the journal. More details about key areas of our scope are below. In all cases authors should include in their article clear rationale for why their research has been carried out.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.