ReviewRSC advances2026
Enantioselective cyclization reactions involving 3-isothiocyanato oxindoles: synthesis of spirocycles.
Review in RSC advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Recently, 3-isothiocyanato oxindoles have been used in various asymmetric cascade cyclization reactions for the synthesis of biologically important spirocyclic compounds. As a powerful and versatile ambiphilic synthon, 3-isothiocyanato oxindoles react effectively with diverse electron-deficient unsaturated bonds through Michael addition/cyclization reactions under organocatalysis or metal catalysis systems. This review highlights catalytic enantioselective cyclization reaction of 3-isothiocyanato oxindoles since 2011, and discusses their mechanistic insights.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.