Reactivity of azafulvenium methides derived from pyrrolo[1,2-c]thiazole-2, 2-dioxides: Synthesis of functionalised pyrroles

Tetrahedron Letters

Volumn 45, Issue 20, 2004, Pages 3889-3893

  Pinho E Melo, Teresa M V D ^a   Soares, Maria I L ^a   Rocha Gonsalves, António M D'A ^a   McNab, Hamish ^b  

^a UNIVERSITY OF COIMBRA   (Portugal)

^b UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

1,3 Dimethyl 5 oxo 5H pyrrolizine 2 carboxylate; 1 Aza benzo f azulene 3 carboxylate; 1 Azafulvenium methides; N and C Vinylpyrroles

Indexed keywords

OXIDE; PYRROLE DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION KINETICS; HEATING; OXIDATION KINETICS; PROTON NUCLEAR MAGNETIC RESONANCE; PYROLYSIS; SYNTHESIS; TEMPERATURE DEPENDENCE;

EID: 1942439961     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.03.111     Document Type: Article

References (13)

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7. 3: C, 68.22; H, 5.72; N, 4.68. Found: C, 68.60; H, 6.07; N, 4.79%.
8. +, 100%), 190 (24), 174 (69), 162 (16), 145 (45) and 117 (16).
9. NMR data in agreement with the NMR spectra reported for other pyrrolizinones in: McNab H. J. Chem. Soc., Perkin Trans. 1. 1987;657-659.
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11. McNab H., Parson S., Stevenson E. J. Chem. Soc., Perkin Trans. 1. 1999;2047-2048.
12. 3: C, 71.90; H, 4.90; N, 5.24. Found: C, 72.27; H, 5.52; N, 5.28.
13. Gross G., Wentrup C. J. Chem. Soc., Perkin Trans. 1. 1982;360-361.