Literature DB >> 17134295

Nitrene equivalent mediated metal-free ring expansions of alkylidenecyclopropanes and an alkylidenecyclobutane.

Yong Liang1, Lei Jiao, Yuanyuan Wang, Yuanyuan Chen, Linge Ma, Jiaxi Xu, Shiwei Zhang, Zhi-Xiang Yu.   

Abstract

The ring expansion of small-ring compounds provides a powerful method for the construction of various cyclic compounds. Herein, nitrene equivalent mediated metal-free ring expansions of alkylidenecyclopropanes (ACPs) and an alkylidenecyclobutane (ACB) were described. In this synthesis, a series of aryl-substituted cyclobutylidene and cyclopentylidene hydrazine derivatives were obtained under mild conditions in moderate to good yields. [reaction: see text]

Entities:  

Year:  2006        PMID: 17134295     DOI: 10.1021/ol062504t

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

Review 1.  Chemistry of polyvalent iodine.

Authors:  Viktor V Zhdankin; Peter J Stang
Journal:  Chem Rev       Date:  2008-12       Impact factor: 60.622

2.  Stereospecific synthesis of alkylidenecyclopropanes via sequential cyclopropene carbomagnesation/1,3-carbon shift.

Authors:  Xiaocong Xie; Zhe Yang; Joseph M Fox
Journal:  J Org Chem       Date:  2010-06-04       Impact factor: 4.354

3.  Cascade synthesis of (E)-2-alkylidenecyclobutanols.

Authors:  J R Falck; Anish Bandyopadhyay; Narender Puli; Abhijit Kundu; L Manmohan Reddy; Deb K Barma; Anyu He; Hongming Zhang; Dhurke Kashinath; Rachid Baati
Journal:  Org Lett       Date:  2009-10-15       Impact factor: 6.005

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.