105418-43-7Relevant articles and documents
Development of an Alkyne Analogue of the de Mayo Reaction: Synthesis of Medium-Sized Carbacycles and Cyclohepta[b]indoles
Tymann, David,Tymann, Dina Christina,Bednarzick, Ulf,Iovkova-Berends, Ljuba,Rehbein, Julia,Hiersemann, Martin
supporting information, p. 15553 - 15557 (2018/11/10)
Embedded medium-sized carbacycles and cyclohepta[b]indoles occur frequently as scaffold elements in natural products and bioactive compounds. Described herein is a conceptionally novel photochemically triggered cascade process to these scaffolds. Key to the cascading ring-expansion process is an unprecedented intramolecular alkyne analogue of the de Mayo reaction.
Synthesis and Structure-Activity Relationships of the Novel Homopropargylamine Antimycotics
Nussbaumer, Peter,Leitner, Ingrid,Stuetz, Anton
, p. 610 - 615 (2007/10/02)
Analogues of the antimycotic allylamine terbinafine were prepared in which the naphthalene and the tert-butylacetylene moieties were preserved, but the spacer between these two groups was varied, and the antifungal activity of the new compounds was evalua