Highly diastereoselective formation of 1,2,3-trisubstituted cyclopropane derivatives

Organic Letters

Volumn 7, Issue 18, 2005, Pages 4057-4059

  Xie, Xingang ^a   Yue, Guoren ^a,c   Tang, Shouchu ^a   Huo, Xing ^a   Liang, Qiren ^a   She, Xuegong ^a,b   Pan, Xinfu ^a  

^a LANZHOU UNIVERSITY   (China)

^b LANZHOU INSTITUTE OF CHEMICAL PHYSICS   (China)

^c HEXI UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 24944509228     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol051653t     Document Type: Article

References (12)

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9. 2 = 0.0788. The X-ray crystallographic structure of 3c is shown in Figure 1. The crystallographic data have been deposited at the Cambrigde Crystallographic Data Center as supplementary publication No. CCDC 222201.
10. Sikorski, W. H.; Reich, H. J. J. Am. Chem. Soc. 2001, 123, 6527-6535.
11. Racemic vinyl expoxides were easily obtained in high yield starting from the corresponding allyl alcohols via m-CPBA epoxidation, Swern oxidation, and wittig olfination sequences; see Supporting Information for details.
12. Frohn, M.; Dalkiewicz, M.; Tu, Y.; Wang, Z. X.; Shi, Y. J. Org. Chem. 1998, 63, 2948-2953.