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Volumn 67, Issue 18, 2011, Pages 3273-3277

Organocatalytic enantioselective multicomponent cascade reaction: Facile access to tetrahydropyridines with C3 all-carbon quaternary stereocenters

Author keywords

Cascade reactions; Multicomponent; Organocatalysis; Quaternary stereocenters; Tetrahydropyridines

Indexed keywords

CARBON; DIETHYL 1 (4 CHLOROPHENYL) 6 ETHYL 1,2,3,4 TETRAHYDRO 3 PROPIONYLPYRIDINE 3,5 DICARBOXYLATE; DIETHYL 3 ACETYL 1 (4 BROMOPHENYL) 1,2,3,4 TETRAHYDRO 6 METHYLPYRIDINE 3,5 DICARBOXYLATE; DIETHYL 3 ACETYL 1 (4 CHLOROPHENYL) 1,2,3,4 TETRAHYDRO 6 METHYLPYRIDINE 3,5 DICARBOXYLATE; DIETHYL 3 ACETYL 1,2,3,4 TETRAHYDRO 1 (4 METHOXYPHENYL) 6 METHYLPYRIDINE 3,5 DICARBOXYLATE; DIETHYL 3 ACETYL 1,2,3,4 TETRAHYDRO 6 METHYL 1 4 TOLYPYRIDINE 3,5 DICARBOXYLATE; DIETHYL 3 ACETYL 1,2,3,4 TETRAHYDRO 6 METHYL 1 PHENYLPYRIDINE 3,5 DICARBOXYLATE; DIETHYL 3 BUTYRYL 1 (4 CHLOROPHENYL) 1,2,3,4 TETRAHYDRO 6 PROPYLPYRIDINE 3,5 DICARBOXYLATE; DIETHYL 3 BUTYRYL 1,2,3,4 TETRAHYDRO 1 (4 METHOXYPHENYL) 6 PROPYLPYRIDINE 3,5 DICARBOXYLATE; DIETHYL 3 BUTYRYL 1,2,3,4 TETRAHYDRO 6 PROPYL 1 4 TOLYLPYRIDINE 3,5 DICARBOXYLATE; DIETHYL 3 HEPTANOYL 6 HEXYL 1,2,3,4 TETRAHYDRO 1 (4 METHOXYPHENYL)PYRIDINE 3,5 DICARBOXYLATE; DIETHYL 6 ETHYL 1,2,3,4 TETRAHYDRO 1 (4 METHOXYPHENYL) 3 PROPIONYLPYRIDINE 3,5 DICARBOXYLATE; DIETHYL 6 ETHYL 1,2,3,4 TETRAHYDRO 3 PROPIONYL 1 4 TOLYLPYRIDINE 3,5 DICARBOXYLATE; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79954416883     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2011.02.047     Document Type: Article
Times cited : (28)

References (63)
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    • For recent reviews on quaternary stereogenic centers, see
    • For recent reviews on quaternary stereogenic centers, see:
  • 58
    • 67650094837 scopus 로고    scopus 로고
    • For a review on the organocatalytic formation of quaternary stereocenters, see: M. Bella, and T. Gasperi Synthesis 2009 1583
    • (2009) Synthesis , pp. 1583
    • Bella, M.1    Gasperi, T.2
  • 59
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    • For selected recent examples regarding the formation of an all-carbon substituted quaternary stereocenter in chiral amine-catalyzed domino reactions, see
    • For selected recent examples regarding the formation of an all-carbon substituted quaternary stereocenter in chiral amine-catalyzed domino reactions, see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.