Negishi cross-couplings in the synthesis of amino acids
Literature Information
William D. G. Brittain, Steven L. Cobb
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
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
DOI: 10.1039/C7PY01591G
CuAAC click chemistry: a versatile approach towards PVDF-based block copolymers
I. Terzic, N. L. Meereboer, K. Loos
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
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
DOI: 10.1039/C7PY01778B
Reversible star assembly of polyolefins using interconversion between boroxine and boronic acid
Ryo Tanaka, Naoki Tonoko, Shin-ichi Kihara, Yuushou Nakayama, Takeshi Shiono
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
DOI: 10.1039/C7PY01938F
Visible light-induced iniferter polymerization of methacrylates enhanced by continuous flow
Maarten Rubens, Phanumat Latsrisaeng
DOI: 10.1039/C7PY01157A
Branching and molar mass analysis of low density polyethylene using the multiple preparative fractionation concept
P. S. Eselem Bungu, H. Pasch
DOI: 10.1039/C7PY02076G
You might also like
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...
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...
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...
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 ...
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...
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...
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...
What are the main uses of 1-Ethyl-7-[2-methyl-6-(4H-1,2,4-triazol-3-yl)-3-pyridinyl]-3,5-dihydropyrazino[2,3-b]pyrazin-2(1H)-one (CAS: 1228013-15-7)?
1-Ethyl-7-[2-methyl-6-(4H-1,2,4-triazol-3-yl)-3-pyridinyl]-3,5-dihydropyrazino[2...
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...
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...
Source Journal
Organic & Biomolecular Chemistry

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.














