- FeCl3 catalyzed Prins-type cyclization for the synthesis of highly substituted indenes: application to the total synthesis of (±)-jungianol and epi-jungianol.
FeCl3 catalyzed Prins-type cyclization for the synthesis of highly substituted indenes: application to the total synthesis of (±)-jungianol and epi-jungianol.
Organic letters (2013-01-16)
Dattatraya H Dethe, Ganesh Murhade
PMID23317410
ABSTRACT
A novel approach was developed for the synthesis of highly substituted indene derivatives, using an FeCl(3) catalyzed Prins-type cyclization reaction which was further applied in the total synthesis of jungianol and epi-jungianol.
MATERIALS
Product Number
Brand
Product Description
Sigma-Aldrich
Iron(III) chloride hexahydrate, puriss. p.a., ACS reagent, crystallized, 98.0-102% (RT)
Pricing and availability is not currently available.
Pricing and availability is not currently available.
Pricing and availability is not currently available.
Pricing and availability is not currently available.
Pricing and availability is not currently available.
Pricing and availability is not currently available.
Pricing and availability is not currently available.
Pricing and availability is not currently available.