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Volumn 129, Issue 16, 2007, Pages 5264-5271

Indium-catalyzed 2-alkenylation of 1,3-dicarbonyl compounds with unactivated alkynes

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; COVALENT BONDS; ETHERS; FUNCTIONAL GROUPS; INDIUM; REGIOSELECTIVITY; SOLVENTS; THIOPHENE;

EID: 34247525499     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0702014     Document Type: Article
Times cited : (106)

References (60)
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    • 3N gave a mixture of products as an α,β-unsaturated form and a β,γ-unsaturated form; see: Nakamura, M.; Fujimoto, T.; Endo, K.; Nakamura, E. Org. Lett. 2004, 6, 4837-4840.
    • 3N gave a mixture of products as an α,β-unsaturated form and a β,γ-unsaturated form; see: Nakamura, M.; Fujimoto, T.; Endo, K.; Nakamura, E. Org. Lett. 2004, 6, 4837-4840.
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    • 3 showed the catalytic activity in the presence of 1 equiv of amine base, such as DBU, to metal triflate to give the corresponding product in 7% and 5%, respectively. This is due to the assistance of the deprotonation reaction to generate the metal enolate intermediate.
    • 3 showed the catalytic activity in the presence of 1 equiv of amine base, such as DBU, to metal triflate to give the corresponding product in 7% and 5%, respectively. This is due to the assistance of the deprotonation reaction to generate the metal enolate intermediate.
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    • 3N decreased the generation of uncharacterized complex byproducts.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.