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Volumn 19, Issue 2, 2013, Pages 716-720

Tert-butyldimethylsilyl-directed highly enantioselective approach to axially chiral α-allenols

Author keywords

allenes; amines; chirality; enantioselectivity; steric hindrance

Indexed keywords

ALLENES; DESILYLATION; ENANTIOSELECTIVE APPROACH; ENANTIOSELECTIVE SYNTHESIS; PROPARGYLIC ALCOHOLS; PROTECTING GROUP; SECONDARY AMINES; STERIC HINDRANCES;

EID: 84871964283     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201201948     Document Type: Article
Times cited : (76)

References (114)
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    • 2, (S)-α,α-diphenylprolinol, and terminal alkynes in toluene for 10 min at 120 °C, followed by addition of aldehydes at room temperature and then gradual heating to 120 °C from room temperature, are very important factors that determine the high ee values and yields for 1-aryl substituted allenes. However, we have not been able to reproduce their results in terms of ee and yield, for example, in the reaction of 1-decyne with benzaldehyde.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.