English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Propyne iminium triflates  1 – 6  react as dipolarophiles in thermal [3 + 2]-cycloadditions with sufficiently electron rich organoazides to form 1,4,5-trisubstituted 1,2,3-triazoles with iminium functionalization. The reactions require rather strong thermal activation, but can be accelerated by microwave irradiation. The regioselectivity of the cycloaddition at the internal acetylenic bond of 3-cyclopropylpropyne and 3-arylpropyne iminium ions ( 1 – 3  and  4 , respectively) is very high, but is lowered in the presence of sterically demanding substituents at the opposite end of the iminium-substituted C,C triple bond. The iminium-functionalized triazoles can easily be transformed into neutral compounds; herein reported is the formation of triazolyl ketones  10  by hydrolysis and of tertiary triazolyldimethyl amines  12  by LiAlH 4  reduction. When the reduction is performed with sodium boranate or sodium cyanoboranate, amine–borane complexes  15  and  16  are obtained.

Iminium-functionalized 1,2,3-triazoles by [3+2] cycloaddition reactions of internal acetylenic iminium triflates with organoazides