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Volumn 31, Issue 7, 2010, Pages 2057-2060

An efficient synthesis of functionalized 1,6-dienes from Baylis-Hillman adducts via a Pd-catalyzed decarboxylative protonation protocol

Author keywords

1,6 dienes; Baylis Hillman adducts; Decarboxylative protonation; Palladium

Indexed keywords


EID: 77954896458     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2010.31.7.2057     Document Type: Article
Times cited : (1)

References (44)
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    • For our recent papers on Pd-catalyzed decarboxylative protonation, allylation, and elimination reactions, see: (a) Gowrisankar, S.; Kim, K. H.; Kim, S. H.; Kim, J. N. Tetrahedron Lett. 2008, 49, 6241-6244.
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    • For the synthesis of cinnamyl bromide derivatives in a stereoselective manner from Baylis-Hillman adducts, see: (a), and further references cited therein
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    • Decarboxylative protonation product 4a must be formed due to trace amounts of moisture in the reaction mixture
    • Decarboxylative protonation product 4a must be formed due to trace amounts of moisture in the reaction mixture.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.