Dess‐martin periodinane: The reactivity of a λ5‐iodane catalyst explained by topological analysis-Reference-Cited by-同舟云学术

Dess‐martin periodinane: The reactivity of a λ5‐iodane catalyst explained by topological analysis

Published:2018-11-27 Issue: Volume: Page:e25838
ISSN:0020-7608
Container-title:International Journal of Quantum Chemistry
language:en
Short-container-title:Int J Quantum Chem

Author:

Tantardini Christian¹²^ORCID,Michalchuk Adam A. L.²³⁴

Affiliation:

1. Center for Electrochemical Energy Storage, SkolTech Skolkovo Institute of Science and Technology Street Nobelya 3, Moscow Russian Federation

2. Chair of Solid State Chemistry, Novosibirsk State University Street Nobelya 3, Novosibirsk Russian Federation

3. EaStCHEM School of ChemistryUniversity of Edinburgh King's Buildings, West Mains Road, Edinburgh United Kingdom

4. EPSRC Center for Continuous Manufacturing and Crystallisation (CMAC), CMAC Future Manufacturing Research HubUniversity of Strathclyde, Technology and Innovation Center Level 6, 99 George Street, Glasgow United Kingdom

Funder

EPSRC

Publisher

Wiley

Subject

Physical and Theoretical Chemistry,Condensed Matter Physics,Atomic and Molecular Physics, and Optics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/qua.25838

Reference85 articles.

1. Chemistry of Polyvalent Iodine

2. Enantioselective Electrophilic Trifluoromethylthiolation of β-Ketoesters: A Case of Reactivity and Selectivity Bias for Organocatalysis

3. A Chiral Hypervalent Iodine(III) Reagent for Enantioselective Dearomatization of Phenols

4. Asymmetric Dearomatizing Spirolactonization of Naphthols Catalyzed by Spirobiindane-Based Chiral Hypervalent Iodine Species

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