메뉴 건너뛰기




Volumn 16, Issue 23, 2014, Pages 6256-6259

Difluoromethylene phosphabetaine as an equivalent of difluoromethyl carbanion

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; BETAINE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; FLUORINATED HYDROCARBON; METHANE; ORGANOPHOSPHORUS COMPOUND;

EID: 84916217150     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol503225s     Document Type: Article
Times cited : (87)

References (45)
  • 14
    • 84897077273 scopus 로고    scopus 로고
    • For electrophilic difluoromethylation involving difluorocarbene, see: Ni, C.; Hu, J. Synthesis 2014, 46, 842-863
    • (2014) Synthesis , vol.46 , pp. 842-863
    • Ni, C.1    Hu, J.2
  • 22
    • 84916232017 scopus 로고    scopus 로고
    • For sulfur reagents, see ref 4.
    • For sulfur reagents, see ref 4.
  • 30
    • 0000672816 scopus 로고    scopus 로고
    • For detailed discussion on ylide 2 and its earlier applications, see
    • For detailed discussion on ylide 2 and its earlier applications, see: Burton, D. J.; Yang, Z.-Y.; Qiu, W. Chem. Rev. 1996, 96, 1641-1716
    • (1996) Chem. Rev. , vol.96 , pp. 1641-1716
    • Burton, D.J.1    Yang, Z.-Y.2    Qiu, W.3
  • 44
    • 55049121808 scopus 로고    scopus 로고
    • According to Mayrs scale, relative electrophilicites (E parameter) of Michael acceptors decrease in the following order for benzylidene derivatives: Meldrums acid (9.15) > malononitrile (9.42) > malonic ester (20.55). See
    • According to Mayrs scale, relative electrophilicites (E parameter) of Michael acceptors decrease in the following order for benzylidene derivatives: Meldrums acid (9.15) > malononitrile (9.42) > malonic ester (20.55). See: Kaumanns, O.; Lucius, R.; Mayr, H. Chem.-Eur. J. 2008, 14, 9675-9682
    • (2008) Chem.-Eur. J. , vol.14 , pp. 9675-9682
    • Kaumanns, O.1    Lucius, R.2    Mayr, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.