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Volumn 56, Issue 17, 2000, Pages 2693-2697

Palladium-catalyzed acetoxylation of cyclic allyl phosphonates in the presence of isopentyl nitrite and using molecular oxygen as final oxidant

Author keywords

3 acetoxy 1 alkenyl phosphonates; Cyclic dialkyl allyl phosphonates; Isopentyl nitrite; Palladium catalyzed acetoxylation

Indexed keywords

ALKENE; NITRITE; PALLADIUM; PHOSPHONIC ACID DERIVATIVE;

EID: 0034697015     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)00172-1     Document Type: Article
Times cited : (11)

References (33)
  • 16
    • 84991418387 scopus 로고    scopus 로고
    • A similar isomerization process was reported for the acetoxylation of β,γ-unsaturated esters, see Ref. 7
    • A similar isomerization process was reported for the acetoxylation of β,γ-unsaturated esters, see Ref. 7.
  • 17
    • 0032223165 scopus 로고    scopus 로고
    • We have already reported an analoguous reaction during the palladium-catalyzed acetoxylation of (2-butenyl)-tert-butyl-phenyl phosphine oxide, see
    • We have already reported an analoguous reaction during the palladium-catalyzed acetoxylation of (2-butenyl)-tert-butyl-phenyl phosphine oxide, see: Attolini, M.; Principato, B.; Peiffer, G.; Maffei, M. Phosphorus, Sulfur, Silicon 1998, 142, 229-238.
    • (1998) Phosphorus, Sulfur, Silicon , vol.142 , pp. 229-238
    • Attolini, M.1    Principato, B.2    Peiffer, G.3    Maffei, M.4
  • 28
    • 0038327985 scopus 로고
    • The problem of dioxygen activation for aerobic palladium-catalyzed acetoxylations or diacetoxylations has received attention from several research groups: (a) For the first successful allylic acetoxylation of cyclic olefins using molecular oxygen, see
    • The problem of dioxygen activation for aerobic palladium-catalyzed acetoxylations or diacetoxylations has received attention from several research groups: (a) For the first successful allylic acetoxylation of cyclic olefins using molecular oxygen, see: Bäckvall, J. E.; Hopkins, R. B.; Grennberg, H.; Mader, M. M.; Awasthi, A. K. J. Am Chem. Soc., 1990, 112, 5160-5166.
    • (1990) J. Am Chem. Soc. , vol.112 , pp. 5160-5166
    • Bäckvall, J.E.1    Hopkins, R.B.2    Grennberg, H.3    Mader, M.M.4    Awasthi, A.K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.