Total synthesis of Sceletium alkaloids (±)-joubertinamine, (±)-epijoubertinamine, (±)-tortuosamine and formal synthesis of (±)-mesembrine, (±)-N-formyltortuosamine-Reference-Cited by-同舟云学术

Total synthesis of Sceletium alkaloids (±)-joubertinamine, (±)-epijoubertinamine, (±)-tortuosamine and formal synthesis of (±)-mesembrine, (±)-N-formyltortuosamine

Published:2016 Issue:11 Volume:40 Page:9432-9440
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Bhosale Viraj A.¹²³⁴⁵,Ukale Dattatraya U.¹²³⁴⁵,Waghmode Suresh B.¹²³⁴⁵

Affiliation:

1. Garware Research Center

2. Department of Chemistry

3. Savitribai Phule Pune University (formerly University of Pune)

4. Pune 411007

5. India

Abstract

An efficient collective formal/total synthesis of Sceletium alkaloids achieved by employing the Wittig olefination–Claisen rearrangement protocol.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/NJ/C6NJ00630B

Reference77 articles.

1. A synthesis of seco-mesembrane alkaloids, (.+-.)-joubertiamine, (.+-.)-joubertinamine, and (.+-.)-epijoubertinamine.

2. Total syntheses of (.+-.)-mesembrine, (.+-.)-joubertinamine, and (.+-.)-N-demethylmesembrenone

3. Sceletium (aizoaceae) alkaloids: total synthesis of racemic mesembranone, joubertinamine and epijoubertinamine

4. The total synthesis of joubertinamine

5. Joubertinamine: a novel seco-mesembrane alkaloid

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