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Volumn 66, Issue 19, 2010, Pages 3490-3498

3,5-Disubstituted 6H-pyrrolo[1,2-c][1,2,3]triazoles from Morita-Baylis-Hillman adducts of propargyl aldehydes

Author keywords

1,3 Dipolar cycloaddition reaction; 6H Pyrrolo 1,2 c 1,2,3 triazoles; 7,8 Dihydro 4H 1,2,3 triazolo 1,5 a indol 5(6H) ones; Azido enynes; Morita Baylis Hillman; Propargyl aldehydes

Indexed keywords

ACETIC ACID DERIVATIVE; ALDEHYDE DERIVATIVE; AZIDE; INDOLE DERIVATIVE; KETONE DERIVATIVE; PYRROLE DERIVATIVE; SODIUM AZIDE; TRIAZOLE DERIVATIVE;

EID: 77950591918     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2010.03.017     Document Type: Article
Times cited : (32)

References (66)
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    • For reviews of the Morita-Baylis-Hillman reaction, see:
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    • For our recent examples, see
    • For our recent examples, see:
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    • For our recent examples, see
    • For our recent examples, see:
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    • For early reports of azidation of the Morita-Baylis-Hillman acetates, see
    • For early reports of azidation of the Morita-Baylis-Hillman acetates, see:
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    • note
    • The (E)-1-azido-3-methylpent-2-en-4-yne do not undergo intramolecular cycloaddition, see: Ref. 10.
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    • note
    • The olefinic proton of 4f and 4l was observed at δ 6.89 and δ 6.75 as each triplet, and two methylene protons were appeared at δ 4.20 and δ 4.18 as each singlet.
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    • note
    • 6 solvent system.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.