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Novel Selective Approach to Terminally Substituted [ n ]Dendralenes
Author(s) -
Polák Peter,
Tobrman Tomáš
Publication year - 2019
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201801522
Subject(s) - synthon , chemistry , electrophile , nucleophile , ring (chemistry) , combinatorial chemistry , conjugated system , ethylene , stereochemistry , organic chemistry , polymer , catalysis
Dendralenes are simple alkenes with cross‐conjugated double bonds that are frequently synthesized due to being potentially valuable building blocks for the synthesis of more complex structures. The synthetic approaches to dendralenes are based on the cross‐coupling reactions of electrophilic and nucleophilic synthons derived from geminally substituted ethylene. Our novel methodology for the synthesis of only terminally substituted [3]‐ and [4]dendralenes, as well as 2,3‐disubstituted buta‐1,3‐dienes, involves the preparation of 1,2‐disubstituted cyclobutenes from readily available 2‐bromocyclobutanone and the subsequent thermal ring‐opening reactions.