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Volumn 54, Issue 28, 2015, Pages 8263-8266

Organocatalytic Activation of the Leaving Group in the Intramolecular Asymmetric SN2′ Reaction

Author keywords

asymmetric catalysis; nucleophilic substitution; organocatalysis; pyrrolidines

Indexed keywords

ALKYLATION; ALLYLATION; CATALYSIS; CHEMICAL ACTIVATION;

EID: 84933525336     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201502831     Document Type: Article
Times cited : (27)

References (56)
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    • For pioneering work in the field of chiral phosphoric acids, see
    • For pioneering work in the field of chiral phosphoric acids, see
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    • In the absence of molecular sieves, hydrolysis of 1
    • In the absence of molecular sieves, hydrolysis of 1da to 1e competed.
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    • Although fluorobenzene was the best solvent when 1e was used in the reaction, no remarkable solvent effect was observed with 1d. See the Supporting Information for details.
    • Although fluorobenzene was the best solvent when 1e was used in the reaction, no remarkable solvent effect was observed with 1d. See the Supporting Information for details.
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    • The allylic compound 1dj alkylated the catalyst to give the phosphoric acid triester, which has no catalytic activity. See Scheme2B.
    • The allylic compound 1dj alkylated the catalyst to give the phosphoric acid triester, which has no catalytic activity. See Scheme2B.
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    • The N-Ts substrate was used because of the low solubility of the N-DNs substrate.
    • The N-Ts substrate was used because of the low solubility of the N-DNs substrate.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.