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Volumn 121, Issue 30, 1999, Pages 7130-7137

Diastereoselectivity in gas-phase hydride reduction reactions of ketones

Author keywords

[No Author keywords available]

Indexed keywords

KETONE DERIVATIVE;

EID: 0033523221     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9910053     Document Type: Article
Times cited : (23)

References (100)
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    • (1982) Pol. J. Chem. , vol.56 , pp. 485
    • Weclas, L.1    Sokolowski, A.2    Burczyk, B.3
  • 76
    • 0000129485 scopus 로고
    • cis-2-tert-Butyl-1,3-dioxan-5-ol and trans-2-tert-butyl-1,3-dioxan-5-ol: Weclas, L.; Sokolowski, A.; Burczyk, B. Pol. J. Chem. 1982, 56, 485. 2-tert-Butyl-1,3-dioxan-5-one: Majewski, M.; Gleave, D. M.; Nowak, P. Can. J. Chem. 1995, 73, 1616. 2-tert-Butyl-1,3-dithian-5-one and cis-and trans-2-tert-butyl-1,3-dithian-5-ol: Eliel, E. L.; Juaristi, E. J. Am. Chem. Soc. 1978, 100, 6114.
    • (1995) Can. J. Chem. , vol.73 , pp. 1616
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    • (1978) J. Am. Chem. Soc. , vol.100 , pp. 6114
    • Eliel, E.L.1    Juaristi, E.2
  • 85
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    • note
    • The absolute total cross sections for the decomposition of 2C, 2T, and 2M were found to be essentially identical at 12 ± 3 Å.
  • 86
    • 0025950454 scopus 로고
    • Extremely bulky reducing agents in solution, such as the trialkyl-borohydrides, display a preference for equatorial attack with 1: Smith, K.; Pelter, A.; Norbury, A. Tetrahedron Lett. 1991, 32, 6243.
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    • Ph.D. Thesis, Purdue University
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    • (1995)
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.