Approaches to obtaining fluorinated α-amino acids

J Moschner, V Stulberg, R Fernandes… - Chemical …, 2019 - ACS Publications
Fluorine does not belong to the pool of chemical elements that nature uses to build organic
matter. However, chemists have exploited the unique properties of fluorine and produced …

2,2,2-Trifluorodiazoethane (CF3CHN2): A Long Journey since 1943

PK Mykhailiuk - Chemical Reviews, 2020 - ACS Publications
2, 2, 2-Trifluorodiazoethane (CF3CHN2) has been proven to be a valuable reagent for the
rapid synthesis of various classes of trifluoromethyl-substituted organic molecules in both …

Difluoromethylation reactions of organic compounds

DE Yerien, S Barata‐Vallejo… - Chemistry–A European …, 2017 - Wiley Online Library
The relevance of the‐CF2H moiety has attracted considerable attention from organic
synthetic and medicinal chemistry communities, because this group can act as a more …

Asymmetric construction of stereogenic carbon centers featuring a trifluoromethyl group from prochiral trifluoromethylated substrates

J Nie, HC Guo, D Cahard, JA Ma - Chemical reviews, 2011 - ACS Publications
Organofluorine chemistry is an area of tremendous expansion. 1 The field of applications is
impressively wide in scope and has the potential to concern all fields of society. Indeed …

Proline Analogues

V Kubyshkin, M Rubini - Chemical Reviews, 2024 - ACS Publications
Within the canonical repertoire of the amino acid involved in protein biogenesis, proline
plays a unique role as an amino acid presenting a modified backbone rather than a side …

Iron‐catalyzed cyclopropanation with trifluoroethylamine hydrochloride and olefins in aqueous media: in situ generation of trifluoromethyl diazomethane

B Morandi, EM Carreira - Angewandte Chemie International Edition, 2010 - infona.pl
Let's avoid the risk! The title transformation has been developed for the synthesis of
trifluoromethyl‐substituted cyclopropane derivatives (see scheme). It avoids the preparation …

Fluorinated diazoalkanes–a versatile class of reagents for the synthesis of fluorinated compounds

L Mertens, RM Koenigs - Organic & Biomolecular Chemistry, 2016 - pubs.rsc.org
Although diazoalkanes find regular application in organic synthesis, the synthesis and
application of their fluorinated homologues was long neglected. First described in 1943 …

Use of a Traceless Activating and Directing Group for the Construction of Trifluoromethylpyrazoles: One‐Pot Transformation of Nitroolefins and Trifluorodiazoethane

Z Chen, Y Zheng, JA Ma - Angewandte Chemie, 2017 - Wiley Online Library
We disclose an efficient one‐pot transformation of trifluorodiazoethane and higher
perfluorinated homologues with various nitroolefins. This method takes advantage of the …

Proline editing: A general and practical approach to the synthesis of functionally and structurally diverse peptides. Analysis of steric versus stereoelectronic effects of 4 …

AK Pandey, D Naduthambi, KM Thomas… - Journal of the …, 2013 - ACS Publications
Functionalized proline residues have diverse applications. Herein we describe a practical
approach, proline editing, for the synthesis of peptides with stereospecifically modified …

Silver-Mediated Cycloaddition of Alkynes with CF3CHN2: Highly Regioselective Synthesis of 3-Trifluoromethylpyrazoles.

F Li, J Nie, L Sun, Y Zheng, JA Ma - Angewandte Chemie, 2013 - search.ebscohost.com
3-Trifluoromethylpyrazole is the core unit of many drugs, agrochemicals, and related
candidates.[1] Among them are Celecoxib and Mavacoxib (antiarthritic), SC-560 (antitumor) …