2016
DOI: 10.1002/chin.201623182
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ChemInform Abstract: Cation‐Directed Enantioselective N‐Functionalization of Pyrroles.

Abstract: Cation-Directed Enantioselective N-Functionalization of Pyrroles. -(ARMSTRONG, R. J.; D'ASCENZIO, M.; SMITH*, M. D.; Synlett 27 (2016) 01, 6-10, http://dx.doi.org/10.1055/s-0035-1560813 ; Chem. Res. Lab., Univ. Oxford, Oxford OX1 3TA, UK; Eng.) -D. Homolka 23-182

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“…Furthermore, we would be remiss not to mention other efficient methods that have been successfully developed for the synthesis of chiral aminals. These include Toste's fluorination-initiated asymmetric cyclization, 27 Smith's asymmetric phase-transfer catalysis, 28 and Zhou's Brønsted acid catalyzed (R-TRIP) synthesis. 29 Each of these approaches contributes uniquely to the diverse toolkit available for the preparation of chiral aminals, highlighting the richness of methodologies in contemporary asymmetric synthesis.…”
Section: Scheme 9 List's Cpa-catalyzed Enantioselective Synthesis Of ...mentioning
confidence: 99%
“…Furthermore, we would be remiss not to mention other efficient methods that have been successfully developed for the synthesis of chiral aminals. These include Toste's fluorination-initiated asymmetric cyclization, 27 Smith's asymmetric phase-transfer catalysis, 28 and Zhou's Brønsted acid catalyzed (R-TRIP) synthesis. 29 Each of these approaches contributes uniquely to the diverse toolkit available for the preparation of chiral aminals, highlighting the richness of methodologies in contemporary asymmetric synthesis.…”
Section: Scheme 9 List's Cpa-catalyzed Enantioselective Synthesis Of ...mentioning
confidence: 99%