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Volumn 51, Issue 30, 2012, Pages 7532-7536

Exploiting the lithiation-directing ability of oxetane for the regioselective preparation of functionalized 2-aryloxetane scaffolds under mild conditions

Author keywords

cross coupling; isotope effects; ortho lithiation; oxetanes; phthalans

Indexed keywords

CROSS-COUPLINGS; ISOTOPE EFFECT; ORTHO-LITHIATION; OXETANES; PHTHALANS;

EID: 84864232085     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201109113     Document Type: Article
Times cited : (46)

References (35)
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    • Interestingly, while alkyllithiums commonly decompose THF, the use of bimetallic bases promotes the selective α-metalation of both THF and tetrahydrothiophene while retaining their cycloanionic structures; see
    • Interestingly, while alkyllithiums commonly decompose THF, the use of bimetallic bases promotes the selective α-metalation of both THF and tetrahydrothiophene while retaining their cycloanionic structures; see:, E. Crosbie, P. García-Álvarez, A. R. Kennedy, J. Klett, R. E. Mulvey, S. D. Robertson, Angew. Chem. 2010, 122, 9578-9581
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    • 2O at 0°C mainly led to the formation of 1,3-dimethyl-1-phenylpent-1-ene, most likely by alkylative reduction of β-lithiated styrene oxide; see also Ref. [24]
    • 2O at 0°C mainly led to the formation of 1,3-dimethyl-1-phenylpent-1-ene, most likely by alkylative reduction of β-lithiated styrene oxide; see also Ref. [24].
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    • Phthalans are a well-known class of compounds with fascinating pharmacological activities; see
    • Phthalans are a well-known class of compounds with fascinating pharmacological activities; see:, X. Xu, F. Song, S. Wang, S. Li, F. Xiao, J. Zhao, Y. Yang, S. Shang, L. Yang, J. Shi, J. Nat. Prod. 2004, 67, 1661-1666.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.