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Volumn 48, Issue 44, 2007, Pages 7865-7869

Organocatalytic highly enantioselective α-selenenylation of aldehydes

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; ALDEHYDE DERIVATIVE; ALPHA PHENYLSELENOALDEHYDE DERIVATIVE; BETA SELENOALCOHOL DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34848856348     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.08.125     Document Type: Article
Times cited : (51)

References (93)
  • 19
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    • For the asymmetric α-selenenylation of aldehydes, see:
    • For the asymmetric α-selenenylation of aldehydes, see:. Paulmier C., Lerouge P., and Paquevent J.-C. Tetrahedron Lett. 29 (1988) 5889
    • (1988) Tetrahedron Lett. , vol.29 , pp. 5889
    • Paulmier, C.1    Lerouge, P.2    Paquevent, J.-C.3
  • 20
    • 84987577779 scopus 로고
    • For the asymmetric α-selenenylation of ketones, see:
    • For the asymmetric α-selenenylation of ketones, see:. Hiroi K., and Sato S. Synthesis (1985) 635
    • (1985) Synthesis , pp. 635
    • Hiroi, K.1    Sato, S.2
  • 29
    • 0034721440 scopus 로고    scopus 로고
    • For selected examples of enamine activation see: (I) Mannich reactions:
    • For selected examples of enamine activation see: (I) Mannich reactions:. List B. J. Am. Chem. Soc. 122 (2000) 9336
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 9336
    • List, B.1
  • 36
    • 0141522552 scopus 로고    scopus 로고
    • (III) α-aminoxylations:
    • (III) α-aminoxylations:. Zhong G. Angew. Chem., Int. Ed. 42 (2003) 4247
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 4247
    • Zhong, G.1
  • 43
    • 34848844448 scopus 로고    scopus 로고
    • (IV) Michael reactions:
    • (IV) Michael reactions:. Alexakis A., and Andrey O. Org. Lett. 2 (2000) 2975
    • (2000) Org. Lett. , vol.2 , pp. 2975
    • Alexakis, A.1    Andrey, O.2
  • 60
    • 33745715054 scopus 로고    scopus 로고
    • For selected examples of iminium activation, see: and references cited therein
    • For selected examples of iminium activation, see:. Lelais G., and Macmillan D.W.C. Aldrichim. Acta 39 (2006) 79 and references cited therein
    • (2006) Aldrichim. Acta , vol.39 , pp. 79
    • Lelais, G.1    Macmillan, D.W.C.2
  • 61
    • 0000497004 scopus 로고    scopus 로고
    • Addition of nitroalkanes:
    • Addition of nitroalkanes:. Hannesian S., and Pham V. Org. Lett. 2 (2000) 2975
    • (2000) Org. Lett. , vol.2 , pp. 2975
    • Hannesian, S.1    Pham, V.2
  • 80
    • 33845336873 scopus 로고    scopus 로고
    • For a polymer supported proline amide catalyzed α-selenenylation of aldehydes, see:
    • For a polymer supported proline amide catalyzed α-selenenylation of aldehydes, see:. Giacalonea F., Gruttadauria M., Marculescua A.M., and Notoa R. Tetrahedron Lett. 48 (2007) 255
    • (2007) Tetrahedron Lett. , vol.48 , pp. 255
    • Giacalonea, F.1    Gruttadauria, M.2    Marculescua, A.M.3    Notoa, R.4
  • 89
    • 34848917108 scopus 로고    scopus 로고
    • note
    • R = major enantiomer 15 min, minor enantiomer 17 min.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.