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Volumn 74, Issue 19, 2009, Pages 7464-7469

Selective functionalization of sp3 C - H bonds adjacent to nitrogen using (diacetoxyiodo)benzene (DIB)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO NITRILES; C-H BOND; CHEMICAL EQUATIONS; COUPLING REACTION; FUNCTIONALIZED; KETO ESTER; MALONATES; NITROALKANES; NITROGEN ATOM; OXIDATIVE COUPLINGS; SELECTIVE FUNCTIONALIZATION; TETRAHYDROISOQUINOLINES;

EID: 70349451712     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo901583r     Document Type: Article
Times cited : (202)

References (64)
  • 1
    • 0242526099 scopus 로고    scopus 로고
    • For recent reviews on C-H activation and functionalization, see: (a)
    • For recent reviews on C-H activation and functionalization, see: (a) Kakiuchi, F.; Chatani, N. Adv. Synth. Catal. 2003, 345, 1077.
    • (2003) Adv. Synth. Catal. , vol.345 , pp. 1077
    • Kakiuchi, F.1    Chatani, N.2
  • 3
    • 65249146649 scopus 로고    scopus 로고
    • For recent reviews on activation of sp3 C-H bonds adjacent to a nitrogen atom, see: (a)
    • For recent reviews on activation of sp3 C-H bonds adjacent to a nitrogen atom, see: (a) Li, C. J. Acc. Chem. Res. 2009, 42, 335.
    • (2009) Acc. Chem. Res. , vol.42 , pp. 335
    • Li, C.J.1
  • 25
    • 70349463744 scopus 로고    scopus 로고
    • note
    • The only example was achieved by electrochemical oxidation, see ref 3a.
  • 37
    • 67749110109 scopus 로고    scopus 로고
    • For Pdcatalyzed dihydroxylations: (j)
    • For Pdcatalyzed dihydroxylations: (j)Wang, A.; Jiang, H.; Chen, H. J. Am. Chem. Soc. 2009, 131, 3846.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 3846
    • Wang, A.1    Jiang, H.2    Chen, H.3
  • 40
    • 34249012488 scopus 로고    scopus 로고
    • HH (ax-ax, trans): 6-14 Hz]. The coupling constants of similar structure, such as (cis and trans)- 2,3-dihydroxypyrans and substituted tetrahydroquinoline, can also be used for reference. For detail, see: (a)
    • HH (ax-ax, trans): 6-14 Hz]. The coupling constants of similar structure, such as (cis and trans)- 2,3-dihydroxypyrans and substituted tetrahydroquinoline, can also be used for reference. For detail, see: (a) Levecque, P.; Gammon, D.; Kinfe, H. H.; Jacobs, P.; De Vos, D.; Sels, B. Org. Biomol. Chem. 2007, 5, 1800.
    • (2007) Org. Biomol. Chem. , vol.5 , pp. 1800
    • Levecque, P.1    Gammon, D.2    Kinfe, H.H.3    Jacobs, P.4    De Vos, D.5    Sels, B.6
  • 43
    • 0001636945 scopus 로고
    • Furthermore, hypervalent iodine(III) reagents promoted dioxygenation of alkenes always afford the cis-products. The mechanism of the formation of the cis-products have been proposed before. For detail, see (d) Also see ref 11
    • Furthermore, hypervalent iodine(III) reagents promoted dioxygenation of alkenes always afford the cis-products. The mechanism of the formation of the cis-products have been proposed before. For detail, see (d) Rebrovic, L.; Koser, G. F. J. Org. Chem. 1984, 49, 2462. Also see ref 11.
    • (1984) J. Org. Chem. , vol.49 , pp. 2462
    • Rebrovic, L.1    Koser, G.F.2
  • 48


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.