An enantio- and diastereoselective approach to indoloquinolizidines in continuous flow

Author:

Chaudhari Moreshwar B.1ORCID,Gupta Prachi1ORCID,Llanes Patricia1,Zhou Leijie1,Zanda Nicola1,Pericàs Miquel A.1ORCID

Affiliation:

1. Institute of Chemical Research of Catalonia (ICIQ), The Barcelona Institute of Science and Technology (BIST), Av. Països Catalans 16, 43007, Tarragona, Spain

Abstract

A solvent-free enantioselective Michael addition mediated by a polymer-supported Jørgensen–Hayashi catalyst and a domino Pictet–Spengler plus lactamisation sequence has been reported in continuous flow.

Funder

Ministerio de Economía y Competitividad

Ministerio de Ciencia e Innovación

Horizon 2020 Framework Programme

H2020 Marie Skłodowska-Curie Actions

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference82 articles.

1. The Alkaloids: Chemistry and Biology , ed. G. A. Cordell , Academic Press , New York , 1998 , vol. 50

2. C.Szántay and K.Honty , in The Chemistry of Heterocyclic Compounds , ed. J. E. Saxton , Wiley , New York , 1994 , vol. 25 , pp. 161–216

3. An Enantioselective Entry to cis-Perhydroisoquinolines

4. Regiospecific and Stereoselective Syntheses of (±)-Reserpine and (−)-Reserpine

5. Straightforward Methodology for the Enantioselective Synthesis of Benzo[a]- and Indolo[2,3-a]quinolizidines

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