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Volumn 108, Issue 8, 2008, Pages 3326-3350

Gold-catalyzed cycloisomerizations of enynes: A mechanistic perspective

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLENE; ETHERS; HYDROCARBONS; ORGANIC COMPOUNDS;

EID: 51049097913     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr0684319     Document Type: Review
Times cited : (1809)

References (316)
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    • Formation of a bicyclo[3.2.0]hept-5-ene via the thermal reaction of a 1,6-fullerenyne was shown to occur through a stepwise diradical reaction mechanism: (a) Martín, N.; Altable, M.; Filippone, S.; Martín-Domenech, Á.; Güell, M.; Solà, M. Angew. Chem., Int. Ed. 2006, 45, 1439.
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    • llb However, this compound actually has a bicyclo[3.2.0]hept-6-ene structure.
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    • For an example of gold-catalyzed methoxycyclization of an allenene, see
    • For an example of gold-catalyzed methoxycyclization of an allenene, see: Luzung, M. R.; Mauleón, P.; Toste, F. D. J. Am. Chem. Soc. 2007, 129, 12402.
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    • Similar cyclobutenes are obtained from the Pt(II)-catalyzed reaction of 1,2-dien-7-ynes: Matsuda, T.; Kadowaki, S.; Goya, T.; Murakami, M. Synlett 2006, 575.
    • Similar cyclobutenes are obtained from the Pt(II)-catalyzed reaction of 1,2-dien-7-ynes: Matsuda, T.; Kadowaki, S.; Goya, T.; Murakami, M. Synlett 2006, 575.


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