메뉴 건너뛰기




Volumn 61, Issue 9, 1996, Pages 3191-3194

Electrochemical formation and dimerization of α-substituted benzyl radicals. Steric effects on dimerization

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0001067936     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo951577f     Document Type: Article
Times cited : (32)

References (54)
  • 2
    • 0011701095 scopus 로고
    • Lund, H., Baizer, M. M., Eds.; Dekker: New York
    • (b) Peters, D. In Organic Electrochemistry, 3rd ed.; Lund, H., Baizer, M. M., Eds.; Dekker: New York, 1991; pp 361-400.
    • (1991) Organic Electrochemistry, 3rd Ed. , pp. 361-400
    • Peters, D.1
  • 10
    • 85087580134 scopus 로고    scopus 로고
    • note
    • 6
  • 11
    • 5244281987 scopus 로고
    • Ph.D. thesis, Wesleyan University
    • Reed, R. G. Ph.D. thesis, Wesleyan University, 1971.
    • (1971)
    • Reed, R.G.1
  • 26
    • 0000293241 scopus 로고
    • Fry A. J.; Sirisoma, U. N. J. Org. Chem. 1993, 58, 4919; 1994, 58, 2914.
    • (1994) J. Org. Chem. , vol.58 , pp. 2914
  • 34
    • 85087581900 scopus 로고    scopus 로고
    • note
    • 23 reported the synthesis of 3c in 1952 without discussion of its stereochemistry; their reported mp of 150-152°C corresponds to the meso diastereomer.
  • 41
    • 0001495715 scopus 로고
    • N2 attack on starting material in electrolyses of alkyl halides; see, e.g., ref 10b and: Fry, A. J.; Fry, P. F. J. Org. Chem. 1993, 58, 3496.
    • (1993) J. Org. Chem. , vol.58 , pp. 3496
    • Fry, A.J.1    Fry, P.F.2
  • 44
    • 5244277757 scopus 로고
    • Thesis, Wesleyan University
    • Powers, T. A. B. A. Thesis, Wesleyan University, 1986.
    • (1986)
    • Powers, T.A.B.A.1
  • 48
    • 5244253479 scopus 로고    scopus 로고
    • Reference 31, pp 701-702
    • (a) Reference 31, pp 701-702.
  • 49
    • 0000430576 scopus 로고
    • (b) The experimental cis-1,3-diaxial dimethyl interaction energy of 3.7 kcal would undoubtedly be far greater (≫100 kcal) except for the distortions which the cyclohexane ring undergoes to minimize the steric repulsion between the two methyl groups: Allinger, N. L.; Miller, M. A. J. Am. Chem. Soc. 1961, 83, 2145.
    • (1961) J. Am. Chem. Soc. , vol.83 , pp. 2145
    • Allinger, N.L.1    Miller, M.A.2
  • 52
    • 5244228795 scopus 로고
    • U. S. Patent 3 420 900
    • Mark, V. U. S. Patent 3 420 900; Chem. Abstr. 1969, 70, 67765s.
    • (1969) Chem. Abstr. , vol.70
    • Mark, V.1
  • 53
    • 5244286412 scopus 로고    scopus 로고
    • note
    • Reference I, Chapter 10. Electrolysis cells were obtained from The Electrochemical Co., 116 Maple Shade Rd., Middletown, CT 06459.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.