Cucurbit[7]uril as a Supramolecular Artificial Enzyme for Diels-Alder Reactions-Reference-Cited by-同舟云学术

Cucurbit[7]uril as a Supramolecular Artificial Enzyme for Diels-Alder Reactions

Published:2017-11-03 Issue:49 Volume:129 Page:15894-15898
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Palma Aniello¹,Artelsmair Markus¹^ORCID,Wu Guanglu¹^ORCID,Lu Xiaoyong²,Barrow Steven J.¹,Uddin Najib³,Rosta Edina³,Masson Eric²,Scherman Oren A.¹^ORCID

Affiliation:

1. Melville Laboratory for Polymer Synthesis Department of Chemistry; University of Cambridge; Lensfield Road Cambridge CB2 1EW UK

2. Department of Chemistry and Biochemistry; Ohio University; Athens Ohio 45701 USA

3. Department of Chemistry; King's College London; London SE1 1DB UK

Funder

H2020 European Research Council

Engineering and Physical Sciences Research Council

Leverhulme Trust

FP7 People: Marie-Curie Actions

American Chemical Society Petroleum Research Fund

Publisher

Wiley

Subject

General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.201706487/fullpdf

Reference43 articles.

1. The structure of SpnF, a standalone enzyme that catalyzes [4 + 2] cycloaddition

2. Natural Diels–Alderases: Elusive and Irresistable

3. Insight into a natural Diels–Alder reaction from the structure of macrophomate synthase

4. Self-Assembled Single-Walled Metal-Helical Nanotube (M-HN): Creation of Efficient Supramolecular Catalysts for Asymmetric Reaction

5. Molecular Barrel by a Hooping Strategy: Synthesis, Structure, and Selective CO2 Adsorption Facilitated by Lone Pair−π Interactions

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