123123-47-7Relevant articles and documents
Asymmetric total synthesis of naturally occurring spirocyclic tetranorsesquiterpenoid lanceolactone A
Acharyya, Ranjan Kumar,Nanda, Samik
, p. 5027 - 5035 (2018/07/25)
Asymmetric total synthesis of naturally occurring γ-butenolide containing [4.4]spiro-tetrahydrofuran lanceolactone A has been reported in the present work. Bimetallic ("Pd-Cu") cascade cyclization was the crucial reaction employed for the construction of the γ-butenolide framework of the natural product. Subsequently, iodocyclization and reductive deiodination through a transfer hydrogenation reaction were applied to access the target molecule in an efficient manner.
Model studies directed toward forskolin: Synthesis of a tricyclic model compound from farnesol
Scherkenbeck,Barth,Thiel,Metten,Heinemann,Welzel
, p. 6325 - 6336 (2007/10/02)
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