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Volumn 70, Issue 7, 2005, Pages 2870-2873

Polymer-supported organotin reagents for regioselective halogenation of aromatic amines

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; HALOGENATION; POLYMERS; REACTION KINETICS; STEREOCHEMISTRY; TIN;

EID: 17044376689     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0480141     Document Type: Article
Times cited : (53)

References (59)
  • 52
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    • note
    • 21
  • 53
    • 17044370836 scopus 로고    scopus 로고
    • Ph.D. Dissertation, University of Bordeaux I
    • Pourcel, M. Ph.D. Dissertation, University of Bordeaux I, 1997; pp 57-66.
    • (1997) , pp. 57-66
    • Pourcel, M.1
  • 54
    • 77956798625 scopus 로고
    • 119Sn chemical shifts are in good agreement with those reported in solution for organotin reagents with similar functionalities. See: (a) Smith, P. J.; Tupciauskas, A. P. Annu. Rep. NMR Spectrosc. 1978, 8, 291-370. (b) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1985, 16, 73-186. (c) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1999, 38, 203-264.
    • (1978) Annu. Rep. NMR Spectrosc. , vol.8 , pp. 291-370
    • Smith, P.J.1    Tupciauskas, A.P.2
  • 55
    • 1542693412 scopus 로고
    • 119Sn chemical shifts are in good agreement with those reported in solution for organotin reagents with similar functionalities. See: (a) Smith, P. J.; Tupciauskas, A. P. Annu. Rep. NMR Spectrosc. 1978, 8, 291-370. (b) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1985, 16, 73-186. (c) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1999, 38, 203-264.
    • (1985) Annu. Rep. NMR Spectrosc. , vol.16 , pp. 73-186
    • Wrackmeyer, B.1
  • 56
    • 33947519316 scopus 로고    scopus 로고
    • 119Sn chemical shifts are in good agreement with those reported in solution for organotin reagents with similar functionalities. See: (a) Smith, P. J.; Tupciauskas, A. P. Annu. Rep. NMR Spectrosc. 1978, 8, 291-370. (b) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1985, 16, 73-186. (c) Wrackmeyer, B. Annu. Rep. NMR Spectrosc. 1999, 38, 203-264.
    • (1999) Annu. Rep. NMR Spectrosc. , vol.38 , pp. 203-264
    • Wrackmeyer, B.1
  • 57
    • 17044397290 scopus 로고    scopus 로고
    • note
    • In liquid phase, organolithium amides are known to be trapped by triorganotin halides to afford the corresponding N-stannylated amines. Because of the high sensitivity of this type of reagent to moisture, MAS NMR characterization of 6a-i was not attempted.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.