A flexible synthesis of privileged structural motifs using the Ollis-Sweeney ammonium ylid rearrangement

Tetrahedron Letters

Volumn 49, Issue 44, 2008, Pages 6286-6288

  Gasiecki, Alan F ^a   Cross, Jeffrey L ^a   Henry, Rodger F ^a   Gracias, Vijaya ^a   Djuric, Stevan W ^a  

^a ABBOTT LABORATORIES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; AMMONIA; SODIUM CHLORIDE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; HYBRID; REACTION ANALYSIS; RING CLOSING METATHESIS; SYNTHESIS;

EID: 51549117052     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.08.055     Document Type: Article

References (8)

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3. Blackburn G.M., Ollis W.D., Smith C., and Sutherland I.O. J. Chem. Soc., Chem. Commun. (1968) 168
4. Sweeney J.B., Tavassoli A., Carter N.B., and Hayes J.F. Tetrahedron 58 (2002) 10113
5. Sweeney J.B., Tavassoli A., and Workman J.A. Tetrahedron 62 (2006) 11506
6. Coates B., Malone J.F., McCarney M.T., and Stevenson P.J. Tetrahedron Lett. 32 (1991) 2827
7. Soldatova S.A., Akbulatov S.V., Gimranova G.S., et al. Chem. Heterocycl. Compd. 41 (2005) 681 Rearrangement of a 4-phenyl didehydropiperidium ylid afforded a mixture of the expected pyrrolidine and a tetrahydroazepine
8. 6, 125.9 MHz, 30 °C) δ 202.5, 142.4, 141.0, 139.4, 133.5, 132.2, 130.0, 129.3 (2 C′s), 129.0, 128.4 (2 C′s), 127.9, 127.5, 126.3, 80.9, 77.2, 53.6, 52.5, 46.7, 40.1, 37.5, 29.1 (3 C′s).