Zhu, Ming-Hui published the artcileDetosylative (Deutero)alkylation of Indoles and Phenols with (Deutero)alkoxides, Application In Synthesis of 2960-93-2, the publication is Organic Letters (2019), 21(17), 7073-7077, database is CAplus and MEDLINE.
An efficient strategy for N/O-(deutero)alkylation of indoles and phenols with alkoxides/alcs. as the alkylation reagents is described. The consecutive detosylation/alkylation transformations feature mild reaction conditions, high ipso-selectivity, and good functional group tolerance (>50 examples). A one-pot selective N-alkylation of unprotected indoles with alcs. and TsCl is also realized. The application of this method is demonstrated by the introduction of isotope-labeled (CD3 and 13CH3) groups using the readily accessible labeled alcs. and the synthesis of pharmaceuticals.
Organic Letters published new progress about 2960-93-2. 2960-93-2 belongs to naphthyridine, auxiliary class Naphthalene,Ether,Other MOF ligands,Organic ligands for MOF materials, name is 2,2′-Dimethoxy-1,1′-binaphthalene, and the molecular formula is C7H5I2NO3, Application In Synthesis of 2960-93-2.
Referemce:
https://en.wikipedia.org/wiki/1,8-Naphthyridine,
1,8-Naphthyridine | C8H6N2 – PubChem