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Volumn 45, Issue 9, 2004, Pages 1865-1868

[2,3]-Wittig rearrangement of methyl β-pyrrolidinyl-γ-allyloxy- (E)-2-butenoate. Expeditious synthesis of 5-alkenyl-4-pyrrolidin-1-yl-5H-furan- 2-ones

Author keywords

2,3 Wittig rearrangement

Indexed keywords

ALKADIENE; BETA PYRROLIDINYL GAMMA ALLYLOXY 2 BUTENOATE; FURAN DERIVATIVE; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 1242316315     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.01.013     Document Type: Article
Times cited : (12)

References (51)
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    • note
    • a signal at 5.54 ppm.
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    • Compounds
    • 4 reduction of the coresponding α,β-unsaturated ester or aldehyde. For the synthesis of the α,β-unsaturated ester or aldehyde, see: Reizelman A., Scheren M., Nefkens G.H.L., Zwanenburg B. Synthesis. 2000;1944-1951.
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    • note
    • 1H NMR signals with syn-13c and anti-13c.
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    • note
    • The crystal structure of compounds syn-13b and syn-13c have been deposited at the Cambridge Crystallographic Data Centre as CCDC 212546 and CCDC 212547.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.