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Volumn 14, Issue 9, 2012, Pages 2242-2245

Pyridine is an organocatalyst for the reductive ozonolysis of alkenes

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; KETONE; OZONE; PYRIDINE; PYRIDINE DERIVATIVE;

EID: 84860635736     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol300617r     Document Type: Article
Times cited : (90)

References (23)
  • 2
    • 0004232165 scopus 로고    scopus 로고
    • Ozonolysis in the Production of Chiral Fine Chemicals. 2 nd ed. Taylor & Francis: Boca Raton, FL, pp 165-184.
    • McGuire, J.; Bond, G.; Haslam, P. J. Ozonolysis in the Production of Chiral Fine Chemicals. Handbook of Chiral Chemicals, 2 nd ed.; Taylor & Francis: Boca Raton, FL, 2006;, pp 165-184.
    • (2006) Handbook of Chiral Chemicals
    • McGuire, J.1    Bond, G.2    Haslam, P.J.3
  • 6
    • 33845375993 scopus 로고
    • see note 27 and references within
    • Lavallee, P; Bouthillier, G. J. Org. Chem. 1986, 51, 1362-5; see note 27 and references within
    • (1986) J. Org. Chem. , vol.51 , pp. 1362-1365
    • Lavallee, P.1    Bouthillier, G.2
  • 12
    • 33749242465 scopus 로고    scopus 로고
    • Tetrahedron 2006, 62, 10747.
    • (2006) Tetrahedron , vol.62 , pp. 10747
  • 16
    • 33746217386 scopus 로고    scopus 로고
    • Lutidine has been employed as an additive for ozonolyses (;), but the substrates in this study would be expected to generate aldehydes regardless of conditions or additives
    • Lutidine has been employed as an additive for ozonolyses (Wang, Y.-G.; Takeyama, R.; Kobayashi, Y. Angew. Chem., Int. Ed. 2006, 45, 3320), but the substrates in this study would be expected to generate aldehydes regardless of conditions or additives
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 3320
    • Wang, Y.-G.1    Takeyama, R.2    Kobayashi, Y.3
  • 18
    • 18744386668 scopus 로고    scopus 로고
    • Pyridine has been applied as an additive to enhance the chemoselectivity of ozonolysis within polyunsaturated systems. See ref 6 and
    • Pyridine has been applied as an additive to enhance the chemoselectivity of ozonolysis within polyunsaturated systems. See ref 6 and: Trost, B. M.; Machacek, M. R.; Tsui, H. C. J. Am. Chem. Soc. 2005, 127, 7014
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 7014
    • Trost, B.M.1    MacHacek, M.R.2    Tsui, H.C.3
  • 21
    • 0037454725 scopus 로고    scopus 로고
    • In contrast, trialkylamines readily decompose terminal ozonides to an aldehyde and formate. and references within
    • In contrast, trialkylamines readily decompose terminal ozonides to an aldehyde and formate. See Hon, Y. S.; Wu, K. C. Tetrahedron 2003, 59, 493 and references within
    • (2003) Tetrahedron , vol.59 , pp. 493
    • See Hon, Y.S.1    Wu, K.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.