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Volumn 12, Issue 13, 2010, Pages 3066-3069

Preparation of tetrasubstituted furans via intramolecular wittig reactions with phosphorus ylides as intermediates

Author keywords

[No Author keywords available]

Indexed keywords

FURAN DERIVATIVE; ORGANOPHOSPHORUS COMPOUND;

EID: 77954097756     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101080q     Document Type: Article
Times cited : (98)

References (56)
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    • To the best of our knowledge, there is no report with phosphorous ylides for the syntheses of furans
    • To the best of our knowledge, there is no report with phosphorous ylides for the syntheses of furans.
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    • For interesting phosphine-mediated reductive cyclizations of γ-acyloxy butynoates to furans, see
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    • In our one-step protocol, the addition sequence of reactants has no influence on the results of the formation of furans
    • In our one-step protocol, the addition sequence of reactants has no influence on the results of the formation of furans.
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    • For another method to prepare the phosphonium enolate zwitterions of type 9 starting from tertiary phosphines, 4-pyridinecarboxaldehyde (3 equiv), and alkynoates (1 equiv) within 0.5-12 h, please see
    • For another method to prepare the phosphonium enolate zwitterions of type 9 starting from tertiary phosphines, 4-pyridinecarboxaldehyde (3 equiv), and alkynoates (1 equiv) within 0.5-12 h, please see
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    • 31P NMR and X-ray analyses (CCDC no. 769222 for 8k, 771901 for 9a, 768638 for 10f, and 746224 for 17)
    • 31P NMR and X-ray analyses (CCDC no. 769222 for 8k, 771901 for 9a, 768638 for 10f, and 746224 for 17).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.