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Volumn , Issue 7, 2001, Pages 1377-1383

An efficient enantioselective entry to the piperidino-quinolizidine ring system of lupine alkaloids by means of n-acyliminium ion initiated cyclization reactions

Author keywords

Alkaloids; Asymmetric synthesis; Cyclization; N ligands

Indexed keywords

3,7 DIAZABICYCLO[3.3.1]NONANE DERIVATIVE; ALKALOID; ION; LUPINE ALKALOID; N ACYLIMINIUM DERIVATIVE; PIPERIDINE DERIVATIVE; QUINOLIZIDINE DERIVATIVE; SILANE DERIVATIVE; UNCLASSIFIED DRUG; VINYL DERIVATIVE; VIRGILIDONE;

EID: 0035066574     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200104)2001:7<1377::aid-ejoc1377>3.3.co;2-6     Document Type: Article
Times cited : (16)

References (42)
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    • note
    • It was not possible to determine the configuration of the C-4 stereogenic centre of 5, neither from the H NMR coupling constants, nor from NOE experiments, due to the severe overlapping between the signals for 4-H and for the benzylic methylene proton signals at δ = 5.1-5.2.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.