Stereo- and Regioselective 1,3-Dipolar Cycloaddition of the Stable Ninhydrin-Derived Azomethine Ylide to Cyclopropenes: Trapping of Unstable Cyclopropene Dipolarophiles-Reference-Cited by-同舟云学术

Stereo- and Regioselective 1,3-Dipolar Cycloaddition of the Stable Ninhydrin-Derived Azomethine Ylide to Cyclopropenes: Trapping of Unstable Cyclopropene Dipolarophiles

Published:2019-05-08 Issue:11 Volume:84 Page:7017-7036
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Filatov Alexander S.¹,Wang Siqi¹,Khoroshilova Olesya V.¹,Lozovskiy Stanislav V.¹,Larina Anna G.¹,Boitsov Vitali M.²³^ORCID,Stepakov Alexander V.¹⁴^ORCID

Affiliation:

1. Institute of Chemistry, Saint Petersburg State University, Universitetsky pr. 26, 198504 St. Petersburg, Russian Federation

2. Saint Petersburg Academic University, ul. Khlopina 8/3, 194021 St. Petersburg, Russian Federation

3. Pavlov First Saint Petersburg State Medical University, ul. L’va Tolstogo 6/8, 197022 St. Petersburg, Russian Federation

4. Saint Petersburg State Institute of Technology, Moskovskii pr. 26, 190013 St. Petersburg, Russian Federation

Funder

Russian Foundation for Basic Research

China Scholarship Council

Russian Academy of Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b00753

Reference72 articles.

1. Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides

2. Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3+2]-Cycloaddition of Azomethine Ylides

3. Recent Advances of Catalytic Asymmetric 1,3-Dipolar Cycloadditions

4. Pyrrolizidine alkaloids

5. Use of nitrogen and oxygen dipole ylides for alkaloid synthesis

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