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Volumn 65, Issue 7, 2009, Pages 1268-1275

Microwave-assisted zinc chloride-catalyzed synthesis of substituted pyrroles from homopropargyl azides

Author keywords

5 endo dig Cyclization; Alkynes; Cyclization; Homopropargyl azides; Nitrogen heterocycles; Pyrroles; Zinc chloride

Indexed keywords

AZIDE; DICHLOROETHANE; PYRROLE DERIVATIVE; ZINC CHLORIDE;

EID: 58149352253     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.11.094     Document Type: Article
Times cited : (36)

References (60)
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    • Recent review:
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    • Selected recent representative examples:
    • Selected recent representative examples:
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    • For halocyclization efforts from this laboratory see:
    • For halocyclization efforts from this laboratory see:
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    • Preparative Acetylenic Chemistry
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    • Recent reviews for Mitsunobu reaction:
    • Recent reviews for Mitsunobu reaction:
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    • See, for example:
    • See, for example:
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    • note
    • Results are summarized in Table S1 (Supplementary data).
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    • note
    • 6O see Ref. 8a.
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    • note
    • 6O cluster is anticipated to be commercially available.
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    • note
    • According to the information from Sigma-Aldrich the solution is prepared using zinc chloride ACS reagent grade >98%, cat. no. #211273.
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    • note
    • HF.
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    • Introduction of the Azido Group
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    • note
    • One signal is obscured.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.