Unusual [3+2] Spiroannulation and Creation of Stereogenic Quaternary Center at C‐3 of Oxindole via Addition of (Het)arynes to Isomerized Morita‐Baylis‐Hillman Adduct of Isatin
Author:
Affiliation:
1. Organic and Bio Organic Chemistry DivisionCSIR-Central Leather Research Institute (CLRI), Adyar Chennai- 600020 INDIA
Funder
CSIR-CLRI
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.201702356
Reference94 articles.
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5. Arynes and Cyclohexyne in Natural Product Synthesis
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2. Synthesis of Spiroindenyl-2-Oxindoles through Palladium-Catalyzed Spirocyclization of 2-Bromoarylamides and Vinyl Bromides;Molecules;2021-12-10
3. o-Silylaryl Triflates: A Journey of Kobayashi Aryne Precursors;Chemical Reviews;2021-02-18
4. Diverse reactivity of isatin-based N,N′-cyclic azomethine imine dipoles with arynes: synthesis of 1′-methyl-2′-oxospiro [indene-1,3′-indolines] and 3-aryl-3-pyrazol-2-oxindoles;New Journal of Chemistry;2020
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