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Volumn 68, Issue 12, 2012, Pages 2679-2686

Enantioselective synthesis of tripodal cyclophanes and pyridinophanes by intramolecular [2+2+2] cycloaddition

Author keywords

Cycloaddition; Cyclophane; Enantioselective; Planar chirality

Indexed keywords

2 AMINOPHENOL; 2,6 (1,2 O BENZO 3 HEPTANO) 4,7 DIPHENYLISOINDOLINE; 2,6 (1,2 O BENZO 3 OXA 7 O PHENYLENEDECANO) 4,7 DIPHENYL 5 (METHOXYMETHYL)ISOINDOLINE; 2,6 (1,2 O BENZO 3 OXAHEPTANO) 2,3 DIHYDRO 4,7 DIMETHYL 1H PYRROLO[3,4 C]PYRIDINE; 2,6 (1,2 O BENZO 3 OXAHEPTANO) 4,7 DIPHENYL 5 METHYLISOINDOLINE; 2,6 (1,2 O BENZO 3 OXAHEXANO) 2,3 DIHYDRO 4,7 DIMETHYL 1H PYRROLO[3,4 C]PYRIDINE; 2,6 (1,2 O BENZO 3 OXANONANO) 2,3 DIHYDRO 4,7 DIMETHYL 1H PYRROLO[3,4 C]PYRIDINE; 2,6 (1,2 O BENZO 3 OXAOCTANO) 2,3 DIHYDRO 4,7 DIMETHYL 1H PYRROLO[3,4 C]PYRIDINE; 2,6 (1,2 O BENZO 3 OXAOCTANO) 2,3 DIHYDRO 4,7 DIPHENYL 1H PYRROLO[3,4 C]PYRIDINE; 2,6 (1,2 O BENZO 3 OXAOCTANO) 4,7 DIPHENYL 5 (METHOXYMETHYL)ISOINDOLINE; 2,6 (1,2 O BENZO 3 OXATETRADECANO) 2,3 DIHYDRO 4,7 DIMETHYL 1H PYRROLO[3,4 C]PYRIDINE; 2,6 (1,2 O BENZO 3 OXATETRADECANO) 2,3 DIHYDRO 4,7 DIPHENYL 1H PYRROLO[3,4 C]PYRIDINE; 2,6 (1,2 O BENZO 3,7 DIOXAOCTANO) 4,7 DIPHENYL 5 METHYLISOINDOLINE; 2,6 [1,4 (1,7 NAPHTHYLENE) 5 OXADECANO] 2,3 DIHYDRO 4,7 DIMETHYL 1H PYRROLO[3,4 C]PYRIDINE; 2,6 [1,4 (1,7 NAPHTHYLENE) 5 OXAUNDECANO] 2,3 DIHYDRO 4,7 DIMETHYL 1H PYRROLO[3,4 C]PYRIDINE; 8 AMINO 2 NAPHTHOL; ALKANE DERIVATIVE; ALKYNE DERIVATIVE; CARBON; CYCLOPHANE DERIVATIVE; NAPHTHALENE DERIVATIVE; NITRILE; OXYGEN; PYRIDINOPHANE DERIVATIVE; TRIYNE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84857631725     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.01.046     Document Type: Article
Times cited : (28)

References (37)
  • 24
    • 69449085237 scopus 로고    scopus 로고
    • The preliminary communication of this work
    • The preliminary communication of this work: T. Shibata, T. Uchiyama, and K. Endo Org. Lett. 11 2009 3906 3908
    • (2009) Org. Lett. , vol.11 , pp. 3906-3908
    • Shibata, T.1    Uchiyama, T.2    Endo, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.