Synthesis of new chiral aziridinoalcohols

Synthetic Communications

Volumn 30, Issue 7, 2000, Pages 1303-1309

  Orea F , L ^a   Galindo, A ^a   Gnecco, D ^a   Toscano, R A ^b   Enriquez R G ^b  

^a BENEMÉRITA UNIVERSIDAD AUTÓNOMA DE PUEBLA   (Mexico)

^b UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; AZIRIDINE DERIVATIVE; GLYCINE DERIVATIVE; PROPIONIC ACID DERIVATIVE;

ARTICLE; CHEMICAL REACTION; DIASTEREOISOMER; ENANTIOMER; RACEMIC MIXTURE; REACTION ANALYSIS; SYNTHESIS;

EID: 0034105149     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397910008087152     Document Type: Article

References (17)

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14. When the reaction was carried out to 95°C; we obtained a complex mixture and the yields of aziridino alcohols were very poor (yields ca. 30%).
15. - Altomare, A.; Cascarano, G.; Giacovazzo, C.; Guagliardi, A.; Burla, M. C.; Polidori, G., and Camalli, M. J. Appl. Cryst. 1994, 27, 435.
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17. - Compounds 6 and 7 exhibit the same MS fragmentation patterns and elemental analysis that 4 and 5 respectively.