On the Extent of Transannular Rearrangement in the Formolysis of 1,5-Cyclooctadiene Monoepoxide

1972 ◽  
Vol 50 (13) ◽  
pp. 2152-2155 ◽  
Author(s):  
John M. McIntosh

Formolysis of 1,5-cyclooctadiene monoepoxide (1) has been shown to give only ca. 25% of products of transannular reactions. The difference between this result and those from the solvolyses of cyclooctene oxide and 4-cyclooctenyl brosylate is attributed to conformational and ring-strain effects.

1974 ◽  
Vol 39 (15) ◽  
pp. 2276-2281 ◽  
Author(s):  
Reuben D. Rieke ◽  
Stephen E. Bales ◽  
Claude F. Meares ◽  
Loretta I. Rieke ◽  
Charles M. Milliren

1971 ◽  
Vol 93 (8) ◽  
pp. 1962-1967 ◽  
Author(s):  
Reuben D. Rieke ◽  
William E. Rich ◽  
Thomas H. Ridgway

1997 ◽  
Vol 38 (35) ◽  
pp. 6177-6180 ◽  
Author(s):  
Michael Schmittel ◽  
Jens-Peter Steffen ◽  
Dominik Auer ◽  
Michael Maywald
Keyword(s):  

2003 ◽  
Vol 1 (5) ◽  
pp. 763-766 ◽  
Author(s):  
Kim K. Baldridge ◽  
Bernadette T. Donovan-Merkert ◽  
Joseph M. O'Connor ◽  
Linda I. Lee ◽  
Adam Closson ◽  
...  

1995 ◽  
Vol 337 (1) ◽  
pp. 60-62 ◽  
Author(s):  
Ralf Harnisch ◽  
Gerlinde Lauterbach ◽  
Wilhelm Pritzkow

Synlett ◽  
2002 ◽  
Vol 2002 (06) ◽  
pp. 0981-0983 ◽  
Author(s):  
A. J. Boydston ◽  
Matthew Laskoski ◽  
Uwe H. F. Bunz ◽  
Michael M. Haley
Keyword(s):  

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