Gold(I)‐Catalyzed Intramolecular Dehydrative Amination of Sulfamate Esters Tethered to Allylic Alcohols: A Strategy for the Synthesis of Cyclic Sulfamidates
Author:
Affiliation:
1. College of Pharmacy & Graduate School of Pharmaceutical Sciences Ewha Womans University 52 Ewhayeodae-gil, Seodaemun-gu Seoul 03760 Republic of Korea
Funder
National Research Foundation of Korea
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202001330
Reference57 articles.
1. Synthesis and reactivity of cyclic sulfamidites and sulfamidates
2. SN2 vs. E2 on quaternary centres: an application to the synthesis of enantiopure β2,2-amino acids
3. One-pot synthesis of functionalized β-amino sulfides/β-amino selenides via ring opening of cyclic sulfamidates
4. 1,2-Cyclic Sulfamidates as Versatile Precursors to Thiomorpholines and Piperazines
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4. Sulfamidate-Based Stereoselective Total Synthesis of (+)-Preussin Using Gold(I)-Catalyzed Intramolecular Dehydrative Amination: Dead End and Detour;The Journal of Organic Chemistry;2023-07-03
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