Radical asymmetric intramolecular α-cyclopropanation of aldehydes towards bicyclo[3.1.0]hexanes containing vicinal all-carbon quaternary stereocenters-Reference-Cited by-同舟云学术

Radical asymmetric intramolecular α-cyclopropanation of aldehydes towards bicyclo[3.1.0]hexanes containing vicinal all-carbon quaternary stereocenters

Published:2018-01-15 Issue:1 Volume:9 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Ye Liu,Gu Qiang-Shuai,Tian Yu,Meng Xiang,Chen Guo-Cong,Liu Xin-Yuan^ORCID

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/s41467-017-02231-7.pdf

Reference70 articles.

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3. Addae-Mensah, I., Waibel, R., Asunka, S. A., Oppong, I. V. & Achenbach, H. The dichapetalins—a new class of triterpenoids. Phytochemistry 43, 649–656 (1996).

4. Li, J. & Lowary, T. L. Synthesis of bicyclo[3.1.0]hexane derivatives as conformationally restricted analogues of β-arabinofuranosyl and α-galactofuranosyl rings. Org. Lett. 10, 881–884 (2008).

5. Toyoda, A. et al. Novel synthesis of 1α,25-dihydroxy-19-norvitamin D from 25-hydroxyvitamin D. Tetrahedron 65, 10002–10008 (2009).

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