A microwave synthesis of the cis and trans isomers of 3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-1,5-benzothiazepin-4(5H)-one : The influence of solvent and power output on the diastereoselectivity

Tetrahedron Letters

Volumn 37, Issue 35, 1996, Pages 6413-6416

  Vega, Juan A ^a   Cueto, Sénida ^a   Ramos, Andrés ^a   Vaquero, Juan J ^a   García Navio, José L ^a   Alvarez Builla, Julio ^a   Ezquerra, Jesus ^b  

^a UNIVERSITY OF ALCALÁ   (Spain)

^b CSIC   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

BENZOTHIAZEPINE DERIVATIVE; DILTIAZEM;

ARTICLE; DRUG SYNTHESIS; MICROWAVE RADIATION; NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; TECHNIQUE;

EID: 0030603056     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01361-5     Document Type: Article

References (31)

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28. 2O (7:3); flow rate: 0.5 mL/min; absorbance: 244 nm; time from injection: trans (10.19 min), cis (13.17 min).
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