Diastereotopic differentiation on phosphorus templates via the ring-closing metathesis reaction

Organic Letters

Volumn 2, Issue 12, 2000, Pages 1769-1772

  Stoianova, Diana S ^a   Hanson, Paul R ^a  

^a UNIVERSITY OF KANSAS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; HETEROCYCLIC COMPOUND; ORGANOPHOSPHORUS COMPOUND; PHOSPHONIC ACID DERIVATIVE;

ARTICLE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

AMIDES; CRYSTALLOGRAPHY, X-RAY; HETEROCYCLIC COMPOUNDS; ORGANOPHOSPHORUS COMPOUNDS; PHOSPHONIC ACIDS; STEREOISOMERISM;

EID: 0034658902     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol005952o     Document Type: Article

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51. 31P NMR compared to the minor diastereoisomers.
52. 31P NMR compared to the minor diastereoisomers. These trends are the same as those seen in the five-membered cyclic phosphonamides 5a-g.
53. 31P NMR compared to the minor diastereoisomers.
54. 1 = Ph, Me) did not improve the selectivity of the reaction.