A novel synthesis of octahydropyrido[3,2- ]carbazole framework of aspidospermidine alkaloids and a combined computational, FT-IR, NMR, NBO, NLO, FMO, MEP study of the cis-4a-Ethyl-1-(2hydroxyethyl)-2,3,4,4a,5,6,7,11c-octahydro-1H-pyrido[3,2-c]carbazole-Reference-Cited by-同舟云学术

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A novel synthesis of octahydropyrido[3,2- ]carbazole framework of aspidospermidine alkaloids and a combined computational, FT-IR, NMR, NBO, NLO, FMO, MEP study of the cis-4a-Ethyl-1-(2hydroxyethyl)-2,3,4,4a,5,6,7,11c-octahydro-1H-pyrido[3,2-c]carbazole

Published:2018-06 Issue: Volume:1161 Page:152-168
ISSN:0022-2860
Container-title:Journal of Molecular Structure
language:en
Short-container-title:Journal of Molecular Structure

Author:

Uludağ Nesimi^ORCID,Serdaroğlu Goncagul^ORCID,Yinanc Abdullah

Funder

Namık Kemal University Scientific

Cumhuriyet University scientific research projects department

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference69 articles.

1. Chapter 1;Sakton,1988

2. The Alkaloids: Chemistry and Physiology;Cordell,1981

3. Revisiting a classic approach to the Aspidosperma alkaloids: an intramolecular Schmidt reaction mediated synthesis of (+)-aspidospermidine;Yengar;J. Org. Chem.,2005

4. Efficient syntheses of (−)-crinine and (−)-aspidospermidine, and the formal synthesis of (−)-minfiensine by enantioselective intramolecular dearomative cyclization

5. Total Synthesis of (+)-Aspidospermidine: A New Strategy for the Enantiospecific Synthesis of Aspidosperma Alkaloids

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