Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/103032
Title: Synthesis of oxacyclic scaffolds via dual ruthenium hydride/Brønsted acid-catalyzed isomerization/cyclization of allylic ethers
Authors: Hansen, Casper L.
Ascic, Erhad
Ohm, Ragnhild G.
Petersen, Rico
Hansen, Mette R.
Madsen, Daniel
Tanner, David
Nielsen, Thomas E.
Keywords: DRNTU::Engineering::Environmental engineering
Issue Date: 2014
Source: Ascic, E., Ohm, R. G., Petersen, R., Hansen, M. R., Hansen, C. L., Madsen, D., et al. (2014). Synthesis of Oxacyclic Scaffolds via Dual Ruthenium Hydride/Brønsted Acid-Catalyzed Isomerization/Cyclization of Allylic Ethers. Chemistry - A European Journal, 20(12), 3297-3300.
Series/Report no.: Chemistry - a European journal
Abstract: A ruthenium hydride/Brønsted acid-catalyzed tandem sequence is reported for the synthesis of 1,3,4,9-tetrahydropyrano[3,4-b]indoles (THPIs) and related oxacyclic scaffolds. The process was designed on the premise that readily available allylic ethers would undergo sequential isomerization, first to enol ethers (Ru catalysis), then to oxocarbenium ions (Brønsted acid catalysis) amenable to endo cyclization with tethered nucleophiles. This methodology provides not only an attractive alternative to the traditional oxa-Pictet–Spengler reaction for the synthesis of THPIs, but also convenient access to THPI congeners and other important oxacycles such as acetals.
URI: https://hdl.handle.net/10356/103032
http://hdl.handle.net/10220/19161
ISSN: 0947-6539
DOI: 10.1002/chem.201304270
Rights: © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SCELSE Journal Articles

SCOPUSTM   
Citations 10

37
Updated on Jan 18, 2023

Web of ScienceTM
Citations 10

38
Updated on Jan 26, 2023

Page view(s) 20

584
Updated on Jan 29, 2023

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.