Stereoselective synthesis of (−)-desethyleburnamonine, (−)-vindeburnol and (−)-3-epitacamonine: observation of a substrate dependent diastereoselectivity reversal of an aldol reaction-Reference-Cited by-同舟云学术

Stereoselective synthesis of (−)-desethyleburnamonine, (−)-vindeburnol and (−)-3-epitacamonine: observation of a substrate dependent diastereoselectivity reversal of an aldol reaction

Published:2016 Issue:44 Volume:14 Page:10394-10406
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Mondal Pravat¹²³⁴,Argade Narshinha P.¹²³⁴

Affiliation:

1. Division of Organic Chemistry

2. National Chemical Laboratory (CSIR)

3. Pune 411 008

4. India

Abstract

(−)-Acetoxyglutarimide was used for synthesis of target compounds wherein an acetoxy group induced enantioselectivity and functioned as a source of ketones.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB01438K

Reference26 articles.

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3. Reserpine: A Challenge for Total Synthesis of Natural Products

4. Synthesis of Strychnine

5. Unified Strategy to Monoterpene Indole Alkaloids: Total Syntheses of (±)-Goniomitine, (±)-1,2-Dehydroaspidospermidine, (±)-Aspidospermidine, (±)-Vincadifformine, and (±)-Kopsihainanine A

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