Asymmetric Total Synthesis of Raputindole D

• Grant number: 13/00642-2
• Support Opportunities: Scholarships in Brazil - Doctorate (Direct)
• Start date: May 01, 2013
• End date: February 28, 2018
• Field of knowledge: Physical Sciences and Mathematics - Chemistry - Organic Chemistry
• Principal Investigator: Joséf Wilhelm Baader
• Grantee: Aline Utaka Scarassati
• Host Institution: Instituto de Química (IQ). Universidade de São Paulo (USP). São Paulo , SP, Brazil

Abstract

Alkaloids bearing the indole moiety constitute one of the most important groups of natural products, mainly due to their remarkable biological activity. Usually, these heterocyclic compounds are substituted in the very reactive two and three positions. In 2010, raputindoles A-D were isolated from the Amazonian plant Raputia simulans Kallunki (Rutaceae), which was collected in Peru. In 2011, a Brazilian research group reported a new analogue for this class of compounds. These bisindoles possess a cyclopentyl unit fused to the benzene ring of one of the indoles and constitute a novel class of indole alkaloids. This project aims to develop a route to the asymmetric synthesis of raputindole D, using hypervalent iodine reagents in the key transformations, including the iodine(III)-mediated ring contraction reaction developed in our research group and an alkynylation using an iodonium salt. The proposed synthesis is convergent and can be easily adapted to other raputindoles.

Academic Publications

(References retrieved automatically from State of São Paulo Research Institutions)

SCARASSATI, Aline Utaka. Studies towards total synthesis of Raputindole D and electrophilic alkynylation of ketones and aldehydes using hypervalent iodine. 2018. Doctoral Thesis - Universidade de São Paulo (USP). Conjunto das Químicas (IQ e FCF) (CQ/DBDCQ) São Paulo.