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Volumn 8, Issue 17, 1997, Pages 2975-2987

Total synthesis of both enantiomers of trans-β-hydroxypipecolic acid

Author keywords

[No Author keywords available]

Indexed keywords

BETA HYDROXYPIPECOLIC ACID; PIPECOLIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0030828305     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(97)00344-3     Document Type: Article
Times cited : (51)

References (39)
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    • note
    • 2, 0°C) were used, a decrease in efficiency and/or diastereoselectivity was observed, being compounds 8 and 9 flanked by two other isomers (diastereomeric ratios ranging from 60:40 to 80:20).
  • 22
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    • note
    • 1H NMR spectrum of an advanced trans-configured piperidine intermediate related to compound 12.
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    • As a rule, lactones having 4R absolute configuration are dextrorotatory, while those having 4S absolute configuration are levorotatory. With few exceptions, this empirical guideline proved widely applicable also to a variety of closely related substances. Casiraghi, G.; Colombo, L.; Rassu, G.; Spanu, P.; Gasparri Fava, G.; Ferrari Belicchi, M. Tetrahedron 1990, 46, 5807.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.