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Volumn 63, Issue 26, 1998, Pages 9968-9977

Reversible charge-accelerated oxy-cope rearrangements

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOL DERIVATIVE; KETONE DERIVATIVE; NORBORNANE DERIVATIVE; OXYGEN;

EID: 0032567294     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo982002w     Document Type: Article
Times cited : (27)

References (34)
  • 1
    • 0000639923 scopus 로고
    • Morrison, J. D., Ed.; Academic Press: New York
    • Review: Hill, R. K. In Asymmetric Synthesis; Morrison, J. D., Ed.; Academic Press: New York, 1984; Vol. 3, p 503.
    • (1984) Asymmetric Synthesis , vol.3 , pp. 503
    • Hill, R.K.1
  • 11
    • 20644448875 scopus 로고
    • Whistler, R. L., BeMiller, J. N., Eds.; Academic Press
    • Stevens, J. D. In Methods in Carbohydrate Chemistry; Whistler, R. L., BeMiller, J. N., Eds.; Academic Press: 1972; Vol. 6, pp 1230-1282.
    • (1972) Methods in Carbohydrate Chemistry , vol.6 , pp. 1230-1282
    • Stevens, J.D.1
  • 21
    • 0344567037 scopus 로고
    • Paquette, L. A., Ed.; John Wiley and Sons: Chichester
    • Gugelchuk, M. In Encyclopedia of Reagents for Organic Synthesis; Paquette, L. A., Ed.; John Wiley and Sons: Chichester, 1995; Vol. 7, pp 4518-4521.
    • (1995) Encyclopedia of Reagents for Organic Synthesis , vol.7 , pp. 4518-4521
    • Gugelchuk, M.1
  • 34
    • 33847529347 scopus 로고    scopus 로고
    • Although 26 and 33 were isolated as single diastereomers, the stereochemistry of their hydroxyl group was not determined because of pending oxidation to the a-diketone. (Tsui, H.-C. Ph.D. Thesis, The Ohio State University, 1998).
    • Although 26 and 33 were isolated as single diastereomers, the stereochemistry of their hydroxyl group was not determined because of pending oxidation to the a-diketone. (Tsui, H.-C. Ph.D. Thesis, The Ohio State University, 1998).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.