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

The reaction between in situ formed 1.1-dichloro-2-neopentyl-1-silene, Cl 2 Si=CHCH 2 tBu (2), and 1,1-dimethylpentafulvene (5) leads to the formation of exo/endo-isomeric [4+2] cycloadducts 9 and [2+2] stereoisomers 10 in good yields. NMR spectroscopic investigations of the product mixture prove the different modes of the silene cycloaddition reactions ([4+2] vs [2+2] addition).

zeitschrift für naturforschung b

Silaheterocyclen, XXXIII [1, 2]: Cycloadditions-Reaktionen des 1.1-Dichlor-2-neopentyIsilaethens mit Pentafulvenen / Silaheterocycles, XXXIII [1, 2]: C y clo ad d itio n Reactions of 1.1-Dichloro-2 -neopentylsilene with Pentafulvenes