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Volumn , Issue 1, 1997, Pages 229-244

Solvolysis of tricyclo[4.1.0.02,7]hept-4-en-3-yl and tricyclo[4.1.0.02,7]hept-3-yl methanesulfonates and p-nitrobenzoates - Remarkably small enthalpy difference between the C7H7 cations tricyclo[4.1.0.02,7]hept-4-en-3-yl and 7-norbornadienyl

Author keywords

4 Halotricyclo 4.1.0.02,7 hept 4 en 3 yl mesylates, solvolysis of; Tricyclo 4.1.0.02,7 hept 3 yl mesylate, solvolysis of; Tricyclo 4.1.0.02,7 hept 4 en 3 yl p nitrobenzoate, solvolysis of

Indexed keywords


EID: 0344111058     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199719970134     Document Type: Article
Times cited : (6)

References (58)
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    • We thank Prof. G. Szeimies for making this information available. The first steps were the addition of dibromocarbene to 1,3-cyclohexadiene (68%) and the epoxidation of the resulting 7,7-dibromobicyclo[4.1.0]hept-2-ene (79%) (R. M. Coates, L. A. Last, J. Am. Chem. Soc. 1983, 105, 7322-7326). In the third step, 7,7-dibromobicyclo[4.1.0]hept-2-ene anti-oxide was converted into 5 (32%) by treatment with two equivalents of butyllithium.
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    • Christl, M.1
  • 22
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    • 2,7]heptyl to anti-7-norbornenyl methyl ether as compared with the solvolysis of anti-7-norbornenyl tosylate (cf.: A. Diaz, M. Brookhart, S. Winstein, J. Am. Chem. Soc. 1966, 88, 3133-3135), if A is indeed an intermediate. (Matrix Presented)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.