Improved Synthetic Utility of a Sluggish Electrophile: Reaction of Chlorosulfonyl Isocyanate with Unreactive and Reactive Alkenes-Reference-Cited by-同舟云学术

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Improved Synthetic Utility of a Sluggish Electrophile: Reaction of Chlorosulfonyl Isocyanate with Unreactive and Reactive Alkenes

Published:2015-04-22 Issue:13 Volume:47 Page:1944-1950
ISSN:0039-7881
Container-title:Synthesis
language:en
Short-container-title:Synthesis

Author:

Shellhamer Dale,Alexander Kelsey,Bunting Summer,Elwin Sarah,Licata Christine,Milligan Jacob,Robinson Ryan,Shipowick Danielle,Smith Lincoln,Perry Marc

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0034-1380553.pdf

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Recent advances in the chemistry of chlorosulfonyl isocyanate: a review;Phosphorus, Sulfur, and Silicon and the Related Elements;2022-04-11

2. One-pot synthesis of oxazolidinones and five-membered cyclic carbonates from epoxides and chlorosulfonyl isocyanate: theoretical evidence for an asynchronous concerted pathway;Beilstein Journal of Organic Chemistry;2020-07-21

3. NMR line-broadening and transverse relaxation time measurements support a di-radical intermediate for the reaction of chlorosulfonyl isocyanate with electron-rich alkenes;Results in Chemistry;2020-01

4. Site-selective enzymatic C‒H amidation for synthesis of diverse lactams;Science;2019-05-10

5. Host defense peptide mimicking poly-β-peptides with fast, potent and broad spectrum antibacterial activities;Biomaterials Science;2019

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