Complexity-Enhancing Acid-Promoted Rearrangement of Tricyclic Products of Tandem Ugi 4CC/Intramolecular Diels−Alder Reaction-Reference-Cited by-同舟云学术

Complexity-Enhancing Acid-Promoted Rearrangement of Tricyclic Products of Tandem Ugi 4CC/Intramolecular Diels−Alder Reaction

Published:2006-11-15 Issue:25 Volume:71 Page:9544-9547
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ilyin Alexei¹,Kysil Volodymyr¹,Krasavin Mikhail¹,Kurashvili Irina¹,Ivachtchenko Alexandre V.¹

Affiliation:

1. Chemical Diversity Research Institute, Khimki, Moscow Reg., 114401 Russia, and ChemDiv, Inc., 11558 Sorrento Valley Road, Suite 5, San Diego, California 92121 av@chemdiv.com

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo061825f

Reference10 articles.

1. A Planning Strategy for Diversity-Oriented Synthesis

2. Exploring New Chemical Space by Stereocontrolled Diversity-Oriented Synthesis

3. Preparation of tricyclic nitrogen heterocycles via tandem four-component condensation/intramolecular Diels-Alder reaction

4. Stereochemical Control of Skeletal Diversity

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