Asset Details
Do you wish to reserve the book?
A novel bis-triazole scaffold accessed via two tandem 3 + 2 cycloaddition events including an uncatalyzed, room temperature azide–alkyne click reaction
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
A novel bis-triazole scaffold accessed via two tandem 3 + 2 cycloaddition events including an uncatalyzed, room temperature azide–alkyne click reaction
Do you wish to request the book?
A novel bis-triazole scaffold accessed via two tandem 3 + 2 cycloaddition events including an uncatalyzed, room temperature azide–alkyne click reaction
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Journal Article
A novel bis-triazole scaffold accessed via two tandem 3 + 2 cycloaddition events including an uncatalyzed, room temperature azide–alkyne click reaction
2022
Overview
The previously described α-acetyl-α-diazomethanesulfonamide was employed in a three-component reaction with azide-containing benzaldehydes and propargylamines. Besides the initial formation of the triazole core, the reaction proceeded further, in uncatalyzed fashion at room temperature and yielded, after intramolecular azide–alkyne click reaction novel, structurally intriguing bistriazoles.
Publisher
Beilstein-Institut zur Föerderung der Chemischen Wissenschaften
Subject
