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Volumn 62, Issue 39, 2006, Pages 9237-9246

Highly enantioselective hydrogenation of exocyclic double bond of N-tosyloxazolidinones catalyzed by a neutral rhodium complex and its synthetic applications

Author keywords

Enantioselective hydrogenation; Exocyclic double bonds; N Tosyloxazolidinones; Rhodium complex

Indexed keywords

AMINO ACID; AMINOALCOHOL; CYCLOOCTANE DERIVATIVE; OXAZOLIDINONE DERIVATIVE; PIPERIDINE DERIVATIVE; RHODIUM COMPLEX;

EID: 33746964416     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.07.024     Document Type: Article
Times cited : (15)

References (46)
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    • For a review on synthetic methods of α-amino acids, see:
    • For a review on synthetic methods of α-amino acids, see:. Duthaler R.O. Tetrahedron 50 (1994) 1539
    • (1994) Tetrahedron , vol.50 , pp. 1539
    • Duthaler, R.O.1
  • 6
    • 33746968694 scopus 로고    scopus 로고
    • For reviews, see:
  • 22
    • 0013603626 scopus 로고
    • The similar phenomena for the asymmetric hydrogenation of geraniol and nerol were reported by Noyori and co-workers.
    • The similar phenomena for the asymmetric hydrogenation of geraniol and nerol were reported by Noyori and co-workers. Inoue S.-I., Osada M., Koyano K., Takaya H., and Noyori R. Chem. Lett. (1985) 1007
    • (1985) Chem. Lett. , pp. 1007
    • Inoue, S.-I.1    Osada, M.2    Koyano, K.3    Takaya, H.4    Noyori, R.5
  • 29
    • 33747009462 scopus 로고    scopus 로고
    • It should be pointed out that 6h and 6i were not hydrogenated under the typical conditions (Table 4).{A figure is presented}
  • 36
    • 33747023073 scopus 로고    scopus 로고
    • The absolute configuration of compound 18 was also assigned as l, namely S by comparison with the optical rotation of literature:
  • 39
    • 33747029479 scopus 로고
    • 23 -37.2 (c 0.62, MeOH)):
    • 23 -37.2 (c 0.62, MeOH)):. Iwata M., and Kuzuhara H. Chem. Lett. (1985) 1941
    • (1985) Chem. Lett. , pp. 1941
    • Iwata, M.1    Kuzuhara, H.2
  • 40


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.