Literature DB >> 17663496

Enantiomerically enriched cyclopropene derivatives: versatile building blocks in asymmetric synthesis.

Ilan Marek1, Samah Simaan, Ahmad Masarwa.   

Abstract

Enantiomerically enriched cyclopropene derivatives, the smallest possible unsaturated carbocycles, are of great synthetic interest since they serve as versatile reactive building blocks. Their reactivity results from the relief of the ring strain in the small molecule. They can be transformed into a wide variety of complex chiral structures and a special emphasis will be directed towards the preparation of enantiomerically enriched methylene- and alkylidenecyclopropane derivatives. The ready availability of a wide range of these chiral entities now provides an excellent opportunity to discover new and unique transformations that can further enrich mainstream synthetic methodology.

Entities:  

Year:  2007        PMID: 17663496     DOI: 10.1002/anie.200604774

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  25 in total

1.  Synthesis of Unusually Strained Spiro Ring Systems and Their Exploits in Synthesis.

Authors:  Richard J Duffy; Kay A Morris; Daniel Romo
Journal:  Tetrahedron       Date:  2009-09-01       Impact factor: 2.457

2.  Studies on the stability of cycloprop-2-ene carboxylate dianions and reactions with electrophiles.

Authors:  Laural A Fisher; Joseph M Fox
Journal:  J Org Chem       Date:  2008-10-14       Impact factor: 4.354

3.  Merging allylic carbon-hydrogen and selective carbon-carbon bond activation.

Authors:  Ahmad Masarwa; Dorian Didier; Tamar Zabrodski; Marvin Schinkel; Lutz Ackermann; Ilan Marek
Journal:  Nature       Date:  2013-12-08       Impact factor: 49.962

4.  Enzymatic construction of highly strained carbocycles.

Authors:  Kai Chen; Xiongyi Huang; S B Jennifer Kan; Ruijie K Zhang; Frances H Arnold
Journal:  Science       Date:  2018-04-06       Impact factor: 47.728

5.  Functionalized Cyclopropenes and Methylenecyclopropenes from Dianions of 3-Hydroxymethylcyclopropenes.

Authors:  Matthew D Hassink; Joseph M Fox
Journal:  Synthesis (Stuttg)       Date:  2012       Impact factor: 3.157

6.  Cyclopropenes in Metallacycle-Mediated Cross-Coupling with Alkynes: Convergent Synthesis of Highly Substituted Vinylcyclopropanes.

Authors:  Natasha F O'Rourke; Glenn C Micalizio
Journal:  Org Lett       Date:  2016-03-01       Impact factor: 6.005

Review 7.  Cycloaddition reactions of enoldiazo compounds.

Authors:  Qing-Qing Cheng; Yongming Deng; Marianne Lankelma; Michael P Doyle
Journal:  Chem Soc Rev       Date:  2017-08-29       Impact factor: 54.564

8.  Facially selective Cu-catalyzed carbozincation of cyclopropenes using arylzinc reagents formed by sequential I/Mg/Zn exchange.

Authors:  Vinod Tarwade; Ramajeyam Selvaraj; Joseph M Fox
Journal:  J Org Chem       Date:  2012-10-19       Impact factor: 4.354

9.  Synthesis of stable derivatives of cycloprop-2-ene carboxylic acid.

Authors:  Ni Yan; Xiaozhong Liu; Mahesh K Pallerla; Joseph M Fox
Journal:  J Org Chem       Date:  2008-05-02       Impact factor: 4.354

10.  Directed carbozincation reactions of cyclopropene derivatives.

Authors:  Vinod Tarwade; Xiaozhong Liu; Ni Yan; Joseph M Fox
Journal:  J Am Chem Soc       Date:  2009-04-22       Impact factor: 15.419

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.