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Volumn 59, Issue 47, 2003, Pages 9255-9303

Recent synthetic uses of functionalised aromatic and heteroaromatic organolithium reagents prepared by non-deprotonating methods

Author keywords

Addition reactions; Aryllithiums; Deprotonations; Halogen lithium exchange; Heteroaryllithiums; Organolithiums; Oxygen lithium exchange; Phosphorous lithium exchange; Selenium lithium exchange; Sulfur lithium exchange; Tellurium lithium exchange

Indexed keywords

2,3 DIHYDRO 2,4,6,7 TETRAMETHYL 2 [(4 PHENYL 1 PIPERIDINYL)METHYL] 5 BENZOFURANAMINE; 3 (3 DIMETHYLAMINOPROPYL) 4 HYDROXY N [4 (4 PYRIDINYL)PHENYL]BENZAMIDE; 3 [6 [7 CYANO 5 (3 FURYL) 2 NAPHTHOXYMETHYL] 2 PYRIDYL] 3 HYDROXY 6,8 DIOXABICYCLO[3.2.1]OCTANE; 6 EPICRININE; ALKALOID DERIVATIVE; ALKENYL GROUP; ALKYL GROUP; ALKYNYL GROUP; AMABILINE; ANSAMYCIN DERIVATIVE; ANTIBIOTIC AGENT; ANTINEOPLASTIC AGENT; AROMATIC COMPOUND; AUGUSTAMINE; BENZOPHENONE DERIVATIVE; CARQUINOSTATIN A; CRININE; ENDOTHELIN A RECEPTOR ANTAGONIST; ESTRADIOL DERIVATIVE; MACBECIN I; MK 287; NAPHTHOQUINONE; NARCICLASINE; NEOCARAZOSTATIN B; NITROGEN; ORGANOLITHIUM COMPOUND; PANCRATISTATIN; SCH 202596; SESQUITERPENE; TEICOPLANIN; THROMBOCYTE ACTIVATING FACTOR ANTAGONIST; UNCLASSIFIED DRUG; UNINDEXED DRUG; UPA 0043; UPA 0044; VANCOMYCIN;

EID: 0242352416     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2003.09.065     Document Type: Review
Times cited : (157)

References (404)
  • 21
    • 0002772829 scopus 로고    scopus 로고
    • For precedent reviews, see: (a) Bailey W.F., Patricia J.J. J. Organomet. Chem. 352:1998;1-46 (b) Parham W.E., Bradsher C.K. Acc. Chem. Res. 15:1982;300-305.
    • (1998) J. Organomet. Chem. , vol.352 , pp. 1-46
    • Bailey, W.F.1    Patricia, J.J.2
  • 22
    • 33845552740 scopus 로고
    • For precedent reviews, see: (a) Bailey W.F., Patricia J.J. J. Organomet. Chem. 352:1998;1-46 (b) Parham W.E., Bradsher C.K. Acc. Chem. Res. 15:1982;300-305.
    • (1982) Acc. Chem. Res. , vol.15 , pp. 300-305
    • Parham, W.E.1    Bradsher, C.K.2
  • 23
    • 85030968954 scopus 로고    scopus 로고
    • Ref. 5b-h are complementary material of this review. During the preparation of this manuscript a review concerning the synthesis of some carbocyclic and heterocyclic systems by a metal-halogen exchange methodology was published:
    • (a) Ref. 5b-h are complementary material of this review. During the preparation of this manuscript a review concerning the synthesis of some carbocyclic and heterocyclic systems by a metal-halogen exchange methodology was published:
  • 31
    • 0034904455 scopus 로고    scopus 로고
    • For recent reviews about arene catalysed lithiations, see: (a) Yus M. Synlett. 2001;1197-1205 (b) Ramón D.J., Yus M. Eur. J. Org. Chem. 2000;225-237 (c) Yus M. Chem. Soc. Rev. 25:1996;155-161.
    • (2001) Synlett , pp. 1197-1205
    • Yus, M.1
  • 32
    • 0033979918 scopus 로고    scopus 로고
    • For recent reviews about arene catalysed lithiations, see: (a) Yus M. Synlett. 2001;1197-1205 (b) Ramón D.J., Yus M. Eur. J. Org. Chem. 2000;225-237 (c) Yus M. Chem. Soc. Rev. 25:1996;155-161.
    • (2000) Eur. J. Org. Chem. , pp. 225-237
    • Ramón, D.J.1    Yus, M.2
  • 33
    • 0030496093 scopus 로고    scopus 로고
    • For recent reviews about arene catalysed lithiations, see: (a) Yus M. Synlett. 2001;1197-1205 (b) Ramón D.J., Yus M. Eur. J. Org. Chem. 2000;225-237 (c) Yus M. Chem. Soc. Rev. 25:1996;155-161.
    • (1996) Chem. Soc. Rev. , vol.25 , pp. 155-161
    • Yus, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.