Lewis Base Catalysis: A Platform for Enantioselective Addition to Alkenes Using Group 16 and 17 Lewis Acids (n → σ*)-Reference-Cited by-同舟云学术

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Lewis Base Catalysis: A Platform for Enantioselective Addition to Alkenes Using Group 16 and 17 Lewis Acids (n → σ*)

Published:2016-08-17 Issue: Volume: Page:1153-1212
ISSN:
Container-title:Lewis Base Catalysis in Organic Synthesis
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Author:

Kalyani Dipannita¹,Kornfilt David J.-P.²,Burk Matthew T.³,Denmark Scott E.²

Affiliation:

1. St. Olaf College; Department of Chemistry; 1520 St. Olaf Ave. Northfield MN 55057 USA

2. University of Illinois; Department of Chemistry, Roger Adams Laboratory; 600 South Mathews Avenue Urbana IL 61801 USA

3. Nalas Engineering; 85 Westbrook Rd Centerbrook CT 06409 USA

Publisher

Wiley-VCH Verlag GmbH & Co. KGaA

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/9783527675142.ch24/fullpdf

Reference206 articles.

1. The Donor-Acceptor Approach to Molecular Interactions

2. Lewis Base Catalysis in Organic Synthesis

3. Chemistry of selenium and tellurium tetrahalides: ionisation of the chlorides and bromides in solution and the constitution of their adducts

4. Unusual attractive interactions between selenium and oxygen in selenoiminoquinones

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1. Cyclopropenium Sulfide as Lewis Base Catalyst for Chemoselective and Regioselective Electrophilic Selenylation of Phenols;ACS Catalysis;2024-06-01

2. Asymmetric Synthesis with Organoselenium Compounds – The Past Twelve Years;Chemistry – A European Journal;2024-02

3. Electronic and Steric Effects on the Reactivity of Seleniranium Ions with Alkenes in the Gas Phase;The Journal of Organic Chemistry;2023-01-27

4. Lewis Base Catalyzed, Sulfenium Ion Initiated Enantioselective, Spiroketalization Cascade;The Journal of Organic Chemistry;2021-10-21

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