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Volumn 131, Issue 46, 2009, Pages 16618-16619

Stereoelectronic effects in vinyl sulfoxides

Author keywords

[No Author keywords available]

Indexed keywords

C-C DOUBLE BONDS; DOUBLE BONDS; ELECTRONWITHDRAWING; LONE PAIR; NUCLEOPHILIC ATTACK; ORBITALS; S-O BONDS; SIGNIFICANT IMPACTS; STEREOELECTRONIC EFFECT; UNSATURATED CARBONYL COMPOUNDS; UV ABSORBANCE; VINYL SULFOXIDE;

EID: 70450192560     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja904354g     Document Type: Article
Times cited : (20)

References (52)
  • 2
    • 0000862670 scopus 로고    scopus 로고
    • Almost a complete issue of Chemical Reviews has been devoted to this highly complex topic: Gung, B. W., le Noble, B., Guest Eds.
    • Almost a complete issue of Chemical Reviews has been devoted to this highly complex topic: Gung, B. W., le Noble, B., Guest Eds. Chem. ReV. 1999, 99 (5), 1067-1480.
    • (1999) Chem. ReV. , vol.99 , Issue.5 , pp. 1067-1480
  • 30
    • 0002377420 scopus 로고
    • By 1973, stereoelectronic effects in vinyl sulfoxides had been explained correctly, albeit without evidence, but these explanations have not been seized in the following decades. See
    • By 1973, stereoelectronic effects in vinyl sulfoxides had been explained correctly, albeit without evidence, but these explanations have not been seized in the following decades. See: Tsuchihashi, G.; Mitamura, S.; Inoue, S.; Ogura, K. Tetrahedron Lett. 1973, 14, 323.
    • (1973) Tetrahedron Lett. , vol.14 , pp. 323
    • Tsuchihashi, G.1    Mitamura, S.2    Inoue, S.3    Ogura, K.4
  • 39
    • 70450188478 scopus 로고    scopus 로고
    • Details are given in the Supporting Information
    • Details are given in the Supporting Information.
  • 44
    • 70450186355 scopus 로고    scopus 로고
    • Zh. Obs. Khim. 2005, 75, 96.
    • (2005) Zh. Obs. Khim. , vol.75 , pp. 96
  • 45
    • 0003622008 scopus 로고    scopus 로고
    • version 3.1; Theoretical Chemistry Institute, University of Wisconsin: Madison, WI
    • Glendening, E. D.; Reed, A. E.; Carpenter, J. E.; Weinhold, F. NBO, version 3.1; Theoretical Chemistry Institute, University of Wisconsin: Madison, WI, 2001.
    • (2001) NBO
    • Glendening, E.D.1    Reed, A.E.2    Carpenter, J.E.3    Weinhold, F.4
  • 49
    • 32944467172 scopus 로고    scopus 로고
    • NBO calculations were performed on structures whose geometries were optimized at the B3LYP/6-31G++(d,p) level of theory using Gaussian 03: 03, revision C.02; Gaussian, Inc.: Wallingford, CT
    • NBO calculations were performed on structures whose geometries were optimized at the B3LYP/6-31G++(d,p) level of theory using Gaussian 03: Frisch, M. J.; et al. Gaussian 03, revision C.02; Gaussian, Inc.: Wallingford, CT, 2004.
    • (2004) Gaussian
    • Frisch, M.J.1
  • 52
    • 70450205681 scopus 로고    scopus 로고
    • A kinetic experiment using sulfoxides 7a and 7b that had a similar outcome is described in the Supporting Information. Isopropylidene derivatives 6 and 8 were not reactive enough, most probably because of steric hindrance
    • A kinetic experiment using sulfoxides 7a and 7b that had a similar outcome is described in the Supporting Information. Isopropylidene derivatives 6 and 8 were not reactive enough, most probably because of steric hindrance.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.