Synthetic chemistry in water: applications to peptide synthesis and nitro-group reductions

Author:

Cortes-Clerget Margery,Lee Nicholas R.,Lipshutz Bruce H.

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology

Reference23 articles.

1. Brown, D. G. & Boström, J. Analysis of past and present synthetic methodologies on medicinal chemistry: where have all the new reactions gone? J. Med. Chem. 59, 4443–4458 (2016).

2. European Chemicals Agency. Member state committee support document for identification of N,N-dimethylformamide as a substance of very high concern because of its CMR properties. ECHA https://echa.europa.eu/documents/10162/13638/supdoc_n_n-dimethylformamide_3204_en.pdf/3f575bea-5a96-4f18-a110-d294d37422c7 (2012).

3. US Environmental Protection Agency. Toxicological review of dichloromethane (methylene chloride). EPA.gov https://cfpub.epa.gov/ncea/iris/iris_documents/documents/toxreviews/0070tr.pdf (2011).

4. Datta, S., Sood, A. & Török, M. A step toward green peptide synthesis. Curr. Org. Synth. 8, 262–280 (2011).

5. Sabatini, M. T., Boulton, L. T. & Sheppard, T. D. Borate esters: simple catalysts for the sustainable synthesis of complex amides. Sci. Adv. 3, e1701028 (2017).

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