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Volumn 35, Issue 20, 1996, Pages 2378-2380

Reductive carbon-suifur bond cleavage: A simple pathway to nonstabilized (lithiomethyl)amines

Author keywords

Amines; Lithium compounds; Metalation; Synthetic methods; Transmetalation

Indexed keywords


EID: 0030471028     PISSN: 05700833     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.199623781     Document Type: Article
Times cited : (22)

References (38)
  • 2
    • 0002191258 scopus 로고
    • Eds.: A.-M. Sapse, P. von R. Schleyer, Wiley, New York
    • b) G. Boche, J. C. W. Lohrenz, A. Opel, Lithium Chemistry (Eds.: A.-M. Sapse, P. von R. Schleyer), Wiley, New York, 1995, pp. 195-226.
    • (1995) Lithium Chemistry , pp. 195-226
    • Boche, G.1    Lohrenz, J.C.W.2    Opel, A.3
  • 3
    • 15744403372 scopus 로고    scopus 로고
    • note
    • α-Heterocarbanions are regarded as stabilized if they carry stabilizing groups on the anionic C atom (e.g. π-systems) or dipole-stabilizing groups, for example acyl groups, on the heteroatom (cf. ref. [1 a]).
  • 4
    • 0001617965 scopus 로고
    • The term carbanion is used for strongly polar organometallic compounds, although it has been known for some time that they do not contain isolated carbanions either in solution or in the solid state. Cf. a) C. Lambert, P. von R. Schleyer, Angew. Chem. 1994, 106, 1187-1199; Angew. Chem. Int. Ed. Engl. 1994, 33, 1129-1141;
    • (1994) Angew. Chem. , vol.106 , pp. 1187-1199
    • Lambert, C.1    Von Schleyer, P.R.2
  • 5
    • 33748633427 scopus 로고
    • The term carbanion is used for strongly polar organometallic compounds, although it has been known for some time that they do not contain isolated carbanions either in solution or in the solid state. Cf. a) C. Lambert, P. von R. Schleyer, Angew. Chem. 1994, 106, 1187-1199; Angew. Chem. Int. Ed. Engl. 1994, 33, 1129-1141;
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 1129-1141
  • 11
    • 33947292664 scopus 로고
    • e) J. Am. Chem. Soc. 1971, 93, 4027-4031;
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 4027-4031
  • 13
    • 0039025928 scopus 로고
    • a) R. Hoffmann, R. Brückner. Angew. Chem. 1992, 104, 646-648; Angew. Chem. Int. Ed. Engl. 1992, 31, 647-649;
    • (1992) Angew. Chem. , vol.104 , pp. 646-648
    • Hoffmann, R.1    Brückner, R.2
  • 14
    • 33748226931 scopus 로고
    • a) R. Hoffmann, R. Brückner. Angew. Chem. 1992, 104, 646-648; Angew. Chem. Int. Ed. Engl. 1992, 31, 647-649;
    • (1992) Angew. Chem. Int. Ed. Engl. , vol.31 , pp. 647-649
  • 21
    • 0000533321 scopus 로고
    • J. Am. Chem. Soc. 1992, 114, 375-377;
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 375-377
  • 25
    • 0000870424 scopus 로고    scopus 로고
    • a) C. Strohmann, Angew. Chem. 1996, 108, 600-601; Angew. Chem. Int. Ed. Engl. 1996, 35, 528-529;
    • (1996) Angew. Chem. , vol.108 , pp. 600-601
    • Strohmann, C.1
  • 26
    • 33748241019 scopus 로고    scopus 로고
    • a) C. Strohmann, Angew. Chem. 1996, 108, 600-601; Angew. Chem. Int. Ed. Engl. 1996, 35, 528-529;
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 528-529
  • 32
    • 15744395542 scopus 로고    scopus 로고
    • Treatment with one equivalent of chloro(dimethyl)phenylsilane gave somewhat diminished yields of 7a-7f
    • Treatment with one equivalent of chloro(dimethyl)phenylsilane gave somewhat diminished yields of 7a-7f.
  • 34
    • 0041473183 scopus 로고    scopus 로고
    • 2Li by hydrogen-lithium exchange and its reactions with chlorosilanes was published: H. H. Karsch, Chem. Ber. 1996, 129, 483-484.
    • (1996) Chem. Ber. , vol.129 , pp. 483-484
    • Karsch, H.H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.