A Short and Efficient Route to Enantiopure 3,5-Diarylpyrrolizidines-Reference-Cited by-同舟云学术

A Short and Efficient Route to Enantiopure 3,5-Diarylpyrrolizidines

Published:1999-02-17 Issue:5 Volume:64 Page:1727-1732
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Scarpi Dina¹,Occhiato Ernesto G.¹,Guarna Antonio¹

Affiliation:

1. Dipartimento di Chimica Organica “U. Schiff” and Centro di Studio sulla Chimica e la Struttura dei Composti Eterociclici e loro Applicazioni, C.N.R., Università di Firenze, Via G. Capponi 9, I-50121 Firenze, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo981946i

Reference27 articles.

1. 2H NMR analysis of the diastereomeric 2-adamantanols-4-d

2. Transformation of 4-nitroalkane-1,7-diones into pyrrolizidines

3. Stereoselektive Synthese von Pyrrolizidin-Alkaloiden aus Nitroalkanonen

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1. Two-directional synthesis as a tool for diversity-oriented synthesis: Synthesis of alkaloid scaffolds;Beilstein Journal of Organic Chemistry;2012-06-06

2. ChemInform Abstract: A Short and Efficient Route to Enantiopure 3,5-Diarylpyrrolizidines.;ChemInform;2010-06-14

3. Diversity-oriented synthesis of bicyclic and tricyclic alkaloids;Chem. Commun.;2010

4. Combining two-directional synthesis and tandem reactions: new access to 3,5-disubstituted pyrrolizidines and first total synthesis of alkaloid cis-223B;Chemical Communications;2009

5. Cis-trans-conversion of the bicycle in pyrrolizidines: The effect of the preferred conformations on the properties of the bases and the thermodynamics of conformational transformation of the ring fusion type. (Review);Chemistry of Heterocyclic Compounds;2006-10