Regio- and chemo-selective cyclization of allenic-Ugi products for the synthesis of 3-pyrroline skeletons-Reference-Cited by-同舟云学术

Regio- and chemo-selective cyclization of allenic-Ugi products for the synthesis of 3-pyrroline skeletons

Published:2019 Issue:39 Volume:17 Page:8858-8870
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Amiri Kamran¹²³⁴^ORCID,Khosravi Hormoz¹²³⁴^ORCID,Balalaie Saeed¹²³⁴⁵^ORCID,Golmohammadi Farhad¹²³⁴,Anwar Muhammad U.⁶⁷⁸⁹^ORCID,Al-Harrasi Ahmed⁶⁷⁸⁹

Affiliation:

1. Peptide Chemistry Research Center

2. K. N. Toosi University of Technology

3. Tehran

4. Iran

5. Medical Biology Research Center

6. Natural and Medical Sciences Research Center

7. University of Nizwa

8. Nizwa

9. Sultanate of Oman

Abstract

A variety of functionalized 3-pyrroline derivatives were prepared by Ugi post-transformation reaction through cyclization of stable allenic-Ugi products in the presence of base at room temperature.

Funder

Alexander von Humboldt-Stiftung

Iran National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB01963D

Reference81 articles.

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4. Cyclization reactions of bis(allenes) for the synthesis of polycarbo(hetero)cycles

5. Expedient syntheses of N-heterocycles via intermolecular amphoteric diamination of allenes

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