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Volumn 56, Issue 33, 2017, Pages 9752-9756

Alkynyl Moiety for Triggering 1,2-Metallate Shifts: Enantiospecific sp2–sp3 Coupling of Boronic Esters with p-Arylacetylenes

Author keywords

1,2 metallate rearrangement; organoboron; phenylacetylenes; sp2 sp3 coupling; stereospecific reactions

Indexed keywords

AROMATIC HYDROCARBONS; BORON; CARBON;

EID: 85023171168     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201703894     Document Type: Article
Times cited : (20)

References (36)
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    • Alkenes can also be used in place of alkynes but reactions are not as clean or high yielding (48 % yield) as the bromohydrin methyl ether was also formed from further bromination of the alkene and trapping by MeOH. See the Supporting Information for details
    • Alkenes can also be used in place of alkynes but reactions are not as clean or high yielding (48 % yield) as the bromohydrin methyl ether was also formed from further bromination of the alkene and trapping by MeOH. See the Supporting Information for details.
  • 17
    • 0000749443 scopus 로고    scopus 로고
    • Angew. Chem. 2001, 113, 2056–2075.
    • (2001) Angew. Chem. , vol.113 , pp. 2056-2075
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    • Angew. Chem. 2007, 119, 7635–7638;
    • (2007) Angew. Chem. , vol.119 , pp. 7635-7638


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.