Rapid access to cis-cyclobutane γ-amino acids in enantiomerically pure form

Tetrahedron Letters

Volumn 52, Issue 12, 2011, Pages 1253-1255

  André, Virginie ^a   Vidal, Anne ^a   Ollivier, Jean ^a   Robin, Sylvie ^a,b   Aitken, David J ^a  

^a UNIVERSITÉ PARIS SACLAY   (France)

^b UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

Amino acids; 2+2 Cycloaddition; Cyclobutanes; Photochemical synthesis; Pyrrolinones

Indexed keywords

2 (AMINOMETHYL)CYCLOBUTANE 1 CARBOXYLIC ACID; AMINO ACID; CARBOXYLIC ACID DERIVATIVE; CYCLOBUTANE; CYCLOBUTANE GAMMA AMINO ACID; ETHYLENE; GAMMA LACTAM DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CYCLOADDITION; PHOTOCHEMISTRY; STEREOISOMERISM;

EID: 79951751982     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.01.013     Document Type: Article

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50. 9). Our spectral and optical rotation data for these compounds were consistent with the literature, and were used to assign the absolute configurations of our compounds.
51. 2O).
52. 2, rt, 90 min) to obtain (-)-9 once again and found it to have an ee of >95% by chiral hplc analysis. We conclude that out collected data are internally coherent and consistent with complete stereochemical integrity of our samples.