Finally we can announce that our moving to Technische Universität Dresden was succesfully. Officially we are at TU since April 1, 2020 but because of the Corona-Pandemia the moving was delayed according to the restrictions. Our group is replacing the Metz group in the Department of Organic Chemistry (Chair of Organic Chemistry I) and we're looking forward to our time in this new scientific surrounding.

Their publication describes the efficient stereoselective hydroboration of internal alkynes using the Fe-H complex FeH(CO)(NO)(PPh₃)₂ and either pinacolborane or bis(pinacolato)diboron. The boron source is essential for a mechanistic dichotomy and therefore for the regioselectivity. Good work, Fabi and Franzi! Congratulations! DOI

A catalytic method for the direct intramolecular amination of aryl vinyl azides to give the corresponding indole derivatives is described. The nucleophilic Fe‐complex Bu4N[Fe(CO)3(NO)] (TBA[Fe]) is used as catalyst and the procedure leads to good to excellent yields. Good work, Asli! Congratulations! DOI

The catalytic cyclopropanation of enynes to substituted propargyl cyclopropanes under thermal/photochemical conditions is described. In this method diazoesters are used as carbene surrogates and the nucleophilic Fe-complex Bu₄N[Fe(CO)₃(NO)] (TBA[Fe]) as catalyst. Good work, Marie! Congratulations! DOI

The catalytic and selective deuteration of polyfunctional organic molecules using [RuCl₂(PPh₃)₃] and D₂O is described. By changing the additive and the amount of zink powder, orthogonal chemoselectivities are observed. Good work, Pascal and Franzi! Congratulations! DOI

Jianan got the Chinese Government Scholarship by the CSC (Chinese Scholarship Council). Congratulations! He will focus on iron complex synthesis and iron-catalysis. We wish you a lot of fun and success!

Arnar is doing his Ph.D. in the Bäckvall group and will work in our group for three month. During this time he will focus on the modification of iron-complexes and their application in cycloisomerizations.

The successful use of the nucleophilic iron complex Bu₄N[Fe(CO)₃(NO)] (TBA[Fe]) as a proton‐transfer catalyst in the cyclocondensation reaction between azides and ketones is reported. The reason for the formation of 1,2,3-triazoles instead of the C−H amination product seems to be a significantly faster proton‐transfer catalysis than the nitrene‐transfer catalysis. An example of a successful sequential Dimroth triazole–indoline synthesis to the corresponding triazole‐substituted indolines is presented. Good work, Asli! Congratulations! DOI

Intramolecular aminations of C–H bonds represent an elegant synthetic way to form important N-heterocycles. Organometallic complexes allow to catalyze the C–H amination under mild conditions. In this review, the most important developments to this field of research concerning Fe-catalysts are summarised and categorized by open-shell (radical) and closed-shell (non-radical) mechanisms. Congratulations! DOI

Lei has successfully defended his Ph.D. thesis. Congratulations and all the best for your future!