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Rhenium-catalysed reactions in chemical synthesis: selected case studies.
Olding, Angus; Tang, Meiqiong; Ho, Curtis C; Fuller, Rebecca O; Bissember, Alex C.
Affiliation
  • Olding A; School of Natural Sciences - Chemistry, University of Tasmania, Hobart, Tasmania, 7001, Australia. curtis.ho@utas.edu.au.
  • Tang M; School of Natural Sciences - Chemistry, University of Tasmania, Hobart, Tasmania, 7001, Australia. curtis.ho@utas.edu.au.
  • Ho CC; School of Natural Sciences - Chemistry, University of Tasmania, Hobart, Tasmania, 7001, Australia. curtis.ho@utas.edu.au.
  • Fuller RO; School of Natural Sciences - Chemistry, University of Tasmania, Hobart, Tasmania, 7001, Australia. curtis.ho@utas.edu.au.
  • Bissember AC; School of Natural Sciences - Chemistry, University of Tasmania, Hobart, Tasmania, 7001, Australia. curtis.ho@utas.edu.au.
Dalton Trans ; 51(8): 3004-3018, 2022 Feb 22.
Article in En | MEDLINE | ID: mdl-35098957
ABSTRACT
This Perspective presents and discusses a selection of examples that reinforce the enabling and distinctive reactivity provided by homogeneous rhenium catalysis in chemical synthesis. Specifically, the ability for lower oxidation state rhenium-carbonyl catalysts to engage alkyne, allene, and enol substrates in various carbon-carbon bond-forming reactions is highlighted. The inherent capacity of Lewis acidic, higher oxidation state oxorhenium catalysts to facilitate the transposition/isomerisation of allyl alcohols and attendant functionalisation via reaction cascades is also showcased. A brief overview of representative rhenium catalysts that have allowed for reductions of imines, carbonyls, and related compounds is also provided.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Dalton Trans Journal subject: QUIMICA Year: 2022 Document type: Article Affiliation country:
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