Novel synthesis of substituted pyrrolidines and piperidines via radical addition-ionic cyclization reaction of oxime ethers

Tetrahedron

Volumn 64, Issue 7, 2008, Pages 1270-1284

  Miyata, Okiko ^a   Takahashi, Shinya ^a   Tamura, Akira ^a   Ueda, Masafumi ^a   Naito, Takeaki ^a  

^a KOBE PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

Indolizidine; Oxime ether; Piperidine; Pyrrolidine; Radical reaction

Indexed keywords

2 (1 METHYLETHYL) 1 (PHENYLMETHOXY)PIPERIDINE; 2 (1 METHYLETHYL) 1 (PHENYLMETHOXY)PYRROLIDINE; 2 (1 METHYLPROPYL) 1 (PHENYLMETHOXY)PIPERIDINE; 2 (1 METHYLPROPYL) 1 (PHENYLMETHOXY)PYRROLIDINE; 2 (2 METHYLPROPYL) 1 (PHENYLMETHOXY)PIPERIDINE; 2 (2 METHYLPROPYL) 1 (PHENYLMETHOXY)PYRROLIDINE; 2 CYCLOHEXYL 1 (PHENYLMETHOXY)PIPERIDINE; 2 CYCLOHEXYL 1 (PHENYLMETHOXY)PYRROLIDINE; 2 CYCLOPENTYL 1 (PHENYLMETHOXY)PIPERIDINE; 2 CYCLOPENTYL 1 (PHENYLMETHOXY)PYRROLIDINE; 2 ETHYL 1 (PHENYLMETHOXY)PIPERIDINE; 2 ETHYL 1 (PHENYLMETHOXY)PYRROLIDINE; 5 (1 METHYLETHYL) 1 (PHENYLMETHOXY) 2 PYRROLIDINONE; 5 (1 METHYLPROPYL) 1 (PHENYLMETHOXY) 2 PYRROLIDINONE; 5 (1,1 DIMETHYLETHYL) 1 (PHENYLMETHOXY) 2 PYRROLIDINONE; 5 (2 METHYLPROPYL) 1 (PHENYLMETHOXY) 2 PYRROLIDINONE; 5 CYCLOHEXYL 1 (PHENYLMETHOXY) 2 PYRROLIDINONE; 5 CYCLOPENTYL 1 (PHENYLMETHOXY) 2 PYRROLIDINONE; 5 ETHYL 1 (PHENYLMETHOXY) 2 PYRROLIDINONE; 5 TRICYCLO[3.3.1.1 3,7]DEC 1 YL 1 (PHENYLMETHOXY) 2 PYRROLIDINONE; 6 (1 METHYLETHYL) 1 (PHENYLMETHOXY) 2 PIPERIDINONE; 6 (1 METHYLPROPYL) 1 (PHENYLMETHOXY) 2 PIPERIDINONE; 6 (1,1 DIMETHYLETHYL) 1 (PHENYLMETHOXY) 2 PIPERIDINONE; 6 (2 METHYLPROPYL) 1 (PHENYLMETHOXY) 2 PIPERIDINONE; 6 ETHYL 1 (PHENYLMETHOXY) 2 PIPERIDINONE; ETHER DERIVATIVE; INDOLIZIDINE DERIVATIVE; OXIME DERIVATIVE; PIPERIDINE DERIVATIVE; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; PRIORITY JOURNAL; RADICAL REACTION; SYNTHESIS;

EID: 37649003075     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.11.081     Document Type: Article

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