Synthesis and photooxygenation of 2-thiofuran derivatives: A mild and direct access to O,S-dimethyl and O-methyl-S-phenyl thiomaleates

Tetrahedron Letters

Volumn 43, Issue 50, 2002, Pages 9129-9132

  Arroyo, Yolanda ^a   Rodríguez, Justo F ^a   Sanz Tejedor, Ma Ascensión ^a   Santos, Mercedes ^a  

^a UNIVERSIDAD DE VALLADOLID   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

MALEIC ACID DERIVATIVE; THIOPHENE DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG SYNTHESIS; PHOTOOXIDATION; PHOTOSENSITIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; PROTON TRANSPORT; STEREOCHEMISTRY;

EID: 0037049207     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02277-3     Document Type: Article

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30. +).
31. 2.
32. +).
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34. There are several reports in which endoperoxides rearranged to give butyrolactones. See Ref. 4a, 5a and (a) Waldemar, A.; Schuhmann, R. M. Liebigs Ann. 1996, 635-640; (b) Freeman-Cook, K. D.; Halcomb, R. L. Tetrahedron Lett. 1998, 39, 8567-8570.