Ring Opening of Aziridines by Pendant Silanols Allows for Stereospecific Preparations of 1′-Amino-tetrahydrofurans
Author:
Affiliation:
1. Department of Medicinal Chemistry, University of Kansas, Lawrence, Kansas 66047, United States
2. Department of Chemistry, Tulane University, New Orleans, Louisiana 70118, United States
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c00763
Reference47 articles.
1. Tethered Silanoxymercuration of Allylic Alcohols
2. A Formal Rearrangement of Allylic Silanols
3. Tethered Silanoxyiodination of Alkenes
4. Unusual rearrangement–remercuration reactions of allylic silanols
5. Ring Opening of Epoxides by Pendant Silanols
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1. Construction of 3‐Substituted Phthalides via Lewis Acid‐Catalyzed Intramolecular Ring Opening of Aziridines with Esters;European Journal of Organic Chemistry;2024-05-06
2. Catalytic Aminium Radical-Cation Salt (Magic Blue)-Initiated SN2-Type Nucleophilic Ring-Opening Transformations of Aziridines;The Journal of Organic Chemistry;2024-02-07
3. Fun With Unusual Functional Groups: Sulfamates, Phosphoramidates, and Di‐tert‐butyl Silanols;European Journal of Organic Chemistry;2024-01-25
4. Ring Opening of Aziridines by Pendant Sulfamates Allows for Regioselective and Stereospecific Preparation of Vicinal Diamines;The Journal of Organic Chemistry;2023-10-30
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