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Volumn 55, Issue 22, 1999, Pages 6883-6904

Synthesis of optically active N-allyl amino compounds with defined trisubstituted double bonds

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLAMINE DERIVATIVE; AZIRIDINE DERIVATIVE; ESTER DERIVATIVE;

EID: 0033612116     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00345-2     Document Type: Article
Times cited : (10)

References (72)
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    • (a) De Meijere, A.; Meyer, F. E. Angew. Chem. 1994, 106, 2473-2506; Angew. Chem. Int. Ed. Engl. 1994, 33, 2379-2412.
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    • (a) Chen, X.-T.; Zou, B.; Bhattacharaya, S. K.; Gutteridge, C. E.; Pettus, T. R. R.; Danishefski, S. J. Angew. Chem. 1998, 110, 835-838; Angew. Chem. Int. Ed. 1998, 37, 789-792.
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    • The cross couplings should be run in presence of triphenylarsane to achieve reaction times less then seven days. Employing triarylphosphanes, more than six weeks were required for a complete conversion of the reacants. (a) Varina, V.; Krishnan, B.; Marshall, D. R.; Roth, G. P. J. Org. Chem. 1993, 58, 5434-5444.
    • (1993) J. Org. Chem. , vol.58 , pp. 5434-5444
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    • 2O was operative, the well known aniline or aminopyridine triflimides (bis-trifluoromethanesulfonyl imides) were found to be less reactive and led to significantly decreased yields, (a) Comins, D. L.; Dehghani, A.; Foti, C. J.; Joseph, S. P. Org. Synth. 1996, 74, 77-81.
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    • The complete maintenance of the chirality can be improved by a Mosher analysis in analogy to ref. 5c and: Dale, D. A.; Dull, D. L.; Mosher, H. S. J. Org. Chem. 1969, 34, 2543-2549.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.