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Volumn 17, Issue 21, 2006, Pages 2981-2986

Conformational control on remote stereochemistry in the intramolecular Pauson-Khand reactions of enynes tethered to homoallyl and homopropargyl alcohols

Author keywords

[No Author keywords available]

Indexed keywords

(3,4A ) 3 (FURAN 2 YL) 3,4,4A,5 TETRAHYDROCYCLOPENTA[C]PYRAN 6(1H) ONE; (3,7A ) 3 (FURAN 2 YL) 3,4,7,7A TETRAHYDROCYCLOPENTA[C]PYRAN 6(1H) ONE; 1 (2 FURYL)BUT 3 EN 1 OL; 1 (2 FURYL)BUT 3 EN 1 YL ACETATE; 1 (FURAN 2 YL)BUT 3 YN 1 OL; 1 (FURAN 2 YL)BUT 3 YNYL ACETATE; 2 (1 (PROP 2 YNYLOXY)BUT 3 ENYL)FURAN; 2 (1 ALLYLOXY)BUT 3 YNYL)FURAN; 2 [1 (ALLYLOXY)BUT 3 YNYL]FURAN; ALLYL ALCOHOL; HOMOALLYL ALCOHOL; HOMOPROPARGYL ALCOHOL;

EID: 33845192880     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2006.11.012     Document Type: Article
Times cited : (10)

References (91)
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    • note
    • 7a,4t
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    • note
    • We applied the conditions given in Ref. 6.
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    • note
    • 13C NMR, FTIR, COSY, HMBC, HMQC and HRMS, and/or elemental analysis. The new chiral center on the final products can be discerned in the X-ray structure relative to homoallylic and homopropargylic alcohols.
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