메뉴 건너뛰기




Volumn , Issue 1, 2009, Pages 129-132

Silver-catalyzed C-H insertion reactions with donor-acceptor diazoacetates

Author keywords

Atom transfer; Chemoselective; Organometallic; Silver; Tris(pyrazolyl)borate

Indexed keywords


EID: 62349112326     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0028-1087377     Document Type: Article
Times cited : (41)

References (47)
  • 45
    • 62349142670 scopus 로고    scopus 로고
    • 2O-PE for ethers) to yield oily transparent or white solid products. The isolated yields are based on the average of at least two experiments and on the amount of diazoacetate used.
    • 2O-PE for ethers) to yield oily transparent or white solid products. The isolated yields are based on the average of at least two experiments and on the amount of diazoacetate used.
  • 47
    • 62349138245 scopus 로고    scopus 로고
    • Methyl 2-Phenyl-3-methylhexanoate: yield: 40.2 mg (73, diastereoisomer ratio, 1.2:1. 1H NMR (300 MHz, CDCl3, δ, 7.19-7.36 (m, 10 H, ArH, 3.624 (s, 3 H, OMe, 3.620 (s, 3 H, OMe, 3.24 (d, J, 10.7 Hz, 1 H, CHPh, 3.23 (d, J, 10.3 Hz, 1 H, CHPh, 2.11-2.28 (m, 2 H, CH, 1.01-1.50 (m, 8 H, CH2, 0.98 (d, J, 6.5 Hz, 3 H, Me, 0.89 (t, J, 6.9 Hz, 3 H, Me, 0.73 (t, J, 6.9 Hz, 3 H, Me, 0.65 (d, J, 6.9 Hz, 3 H, Me, 13C NMR (125 MHz, CDCl3, δ, 174.54, 174.49, 138.19, 138.14, 128.61, 128.58, 128.42, 128.39, 127.14, 58.8, 55.5, 51.7, 37.6, 36.2, 36.1, 35.6, 19.9, 19.4, 17.8, 16.6, 14.2, 14.0. IR (neat, 3087, 3064, 3029, 2959, 2932, 2873, 1738 cm-1. HRMS ESI, m/z [M, H, calcd for C14H21O2: 221.1536; found: 221.1537
    • 2: 221.1536; found: 221.1537.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.