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Volumn 351, Issue 1-2, 2009, Pages 85-88

A dramatic substituent effect in silver(I)-catalyzed regioselective cyclization of ortho-alkynylaryl aldehyde oxime derivatives

Author keywords

Alkynes; Cyclization; Regioselectivity; Silver

Indexed keywords


EID: 58549084996     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200800568     Document Type: Article
Times cited : (94)

References (56)
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    • Many chemists have contributed to this field, but only 1-2 typical examples were selected here from each group, see: a G. Dyker, D. Hildebrandt, J. Liu, K. Merz, Angew. Chem. 2003, 115, 4536;
    • Many chemists have contributed to this field, but only 1-2 typical examples were selected here from each group, see: a) G. Dyker, D. Hildebrandt, J. Liu, K. Merz, Angew. Chem. 2003, 115, 4536;
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    • imine analogue, see: i N. Asao, S. Y. S. T. Nogami, Y. Yamamoto, Angew. Chem. 2005, 117, 5662;
    • imine analogue, see: i) N. Asao, S. Y. S. T. Nogami, Y. Yamamoto, Angew. Chem. 2005, 117, 5662;
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    • 1,2-Allenes, 1,3-dienes and 4H-pyrans could be produced selectively by reacting electron-deficient 1,3-conjugated enynes with different nucleophiles, see: X. Yu, H. Ren, Y. Xiao, J. Zhang, Chem. Eur. J. 2008, ASAP.
    • 1,2-Allenes, 1,3-dienes and 4H-pyrans could be produced selectively by reacting electron-deficient 1,3-conjugated enynes with different nucleophiles, see: X. Yu, H. Ren, Y. Xiao, J. Zhang, Chem. Eur. J. 2008, ASAP.
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    • During our study of this PSCR, Ag(I)-catalyzed cyclization of ortho-alkynylaryl aldehyde oxime leading to isoquinoline N-oxides was published by Seunghoon Shin, see: H.-S. Yeom, S. Kim, S. Shin, Synlett 2008, 924;
    • During our study of this PSCR, Ag(I)-catalyzed cyclization of ortho-alkynylaryl aldehyde oxime leading to isoquinoline N-oxides was published by Seunghoon Shin, see: H.-S. Yeom, S. Kim, S. Shin, Synlett 2008, 924;
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    • for an electrophiles-mediated version of this cyclization to afford the corresponding 4-halide-isoquinoline N-oxides, see: Q. Ding, J. Wu, Adv. Synth. Catal. 2008, 350, 1850.
    • for an electrophiles-mediated version of this cyclization to afford the corresponding 4-halide-isoquinoline N-oxides, see: Q. Ding, J. Wu, Adv. Synth. Catal. 2008, 350, 1850.
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    • Functionalized isoquinolines are an important class of heterocylic compounds with many bioactive activities, see: a The Chemistry of Heterocyclic Compounds: Isoqinolines, Eds, G. M. Coppola, H. F. Schuster, John Wiley & Sons, New York, 1981, 38, Part 3;
    • Functionalized isoquinolines are an important class of heterocylic compounds with many bioactive activities, see: a) The Chemistry of Heterocyclic Compounds: Isoqinolines, (Eds.: G. M. Coppola, H. F. Schuster), John Wiley & Sons, New York, 1981, Vol. 38, Part 3;
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    • Methods for synthesis of isoquinolin-1(2H)-ones, see: a) V. R. Batchu, D. K. Barange, D. Kumar, B. R. Sreekanth, K. Vyas, E. A. Reddy, M. Pal, Chem. Commun. 2007, 1966;
    • Methods for synthesis of isoquinolin-1(2H)-ones, see: a) V. R. Batchu, D. K. Barange, D. Kumar, B. R. Sreekanth, K. Vyas, E. A. Reddy, M. Pal, Chem. Commun. 2007, 1966;


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.