Thermally-induced intramolecular [2 + 2] cycloaddition of acrylamide-tethered alkylidenecyclopropanes-Reference-Cited by-同舟云学术

Thermally-induced intramolecular [2 + 2] cycloaddition of acrylamide-tethered alkylidenecyclopropanes

Published:2018 Issue:35 Volume:16 Page:6399-6404
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zhang Xiao-Yu¹²³⁴,Yang Song¹²³⁴,Wei Yin⁵⁶⁷⁸⁹^ORCID,Shi Min¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory for Advanced Materials and Institute of Fine Chemicals

2. East China University of Science and Technology

3. Shanghai

4. China

5. State Key Laboratory of Organometallic Chemistry

6. Center for Excellence in Molecular Synthesis

7. Shanghai Institute of Organic Chemistry

8. Chinese Academy of Sciences

9. Shanghai 200032

Abstract

Thermally-induced intramolecular [2 + 2] cycloadditions of acrylamide-tethered alkylidenecyclopropanes to generate a series of novel cyclobutane-containing spiro[2.3]hexanes were disclosed.

Funder

Chinese Academy of Sciences

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB01765D

Reference61 articles.

1. Enantiomerically Pure Cyclobutane Derivatives and Their Use in Organic Synthesis

2. The Application of Cyclobutane Derivatives in Organic Synthesis

3. Design of Spiro[2.3]hex-1-ene, a Genetically Encodable Double-Strained Alkene for Superfast Photoclick Chemistry

4. Discovery and Optimization of Potent GPR40 Full Agonists Containing Tricyclic Spirocycles

5. Exploring the Reactivity ofN-Alkynylated Sulfoximines: [2 + 2]-Cycloadditions

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