Stereoselective construction of a 5-aza-spiro[2,4]heptane motif via catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides and ethyl cyclopropylidene acetate

Chemical Communications

Volumn 47, Issue 9, 2011, Pages 2616-2618

  Liu, Tang Lin ^a   He, Zhao Lin ^a   Tao, Hai Yan ^a   Cai, Yue Peng ^b,c   Wang, Chun Jiang ^a,b  

^a WUHAN UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^c SOUTH CHINA NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

5 AZA SPIRO[2,4]HEPTANE; ACETIC ACID DERIVATIVE; AZOMETHINE YLIDE; ETHYL CYCLOPROPYLIDENE ACETATE; HEPTANE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CYCLOADDITION; DIASTEREOISOMER; ENANTIOSELECTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS;

EID: 79952274301     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c0cc04329j     Document Type: Article

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