메뉴 건너뛰기




Volumn , Issue 4, 2004, Pages 679-683

HIV protease inhibitor part 1: Use of Evans' oxazolidinone in intermolecular Diels-Alder reaction en route to 3,4-substituted cyclohexanones

Author keywords

Cyclohexane; Cyclohexanone; Diels Alder; HIV protease inhibitor; Oxazolidinone

Indexed keywords

CYCLOHEXANONE DERIVATIVE; OXAZOLIDINONE DERIVATIVE; PROTEINASE; PROTEINASE INHIBITOR; SAQUINAVIR;

EID: 1642301290     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2004-815438     Document Type: Article
Times cited : (7)

References (28)
  • 11
    • 0025328745 scopus 로고
    • (11) See for example: (a) Damon, R. E.; Coppola, G. M. Tetrahedron Lett. 1990, 31, 2849. (b) Some success has been obtained using α,β;- unsaturated oxazolidinones as dienophiles at r.t. under high pressure in the presence of chiral Lewis acids: Knol, J.; Meetsma, A.; Feringa, B. L. Tetrahedron: Asymmetry 1995, 6, 1069; and references cited therein.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 2849
    • Damon, R.E.1    Coppola, G.M.2
  • 12
    • 0029000081 scopus 로고
    • and references cited therein
    • See for example: (a) Damon, R. E.; Coppola, G. M. Tetrahedron Lett. 1990, 31, 2849. (b) Some success has been obtained using α,β;-unsaturated oxazolidinones as dienophiles at r.t. under high pressure in the presence of chiral Lewis acids: Knol, J.; Meetsma, A.; Feringa, B. L. Tetrahedron: Asymmetry 1995, 6, 1069; and references cited therein.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 1069
    • Knol, J.1    Meetsma, A.2    Feringa, B.L.3
  • 22
    • 1642307655 scopus 로고    scopus 로고
    • note
    • CCDC No. 217034 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/ conts/ retrieving.html [or from the CCDC 12 Union Road Cambridge CB2 1EZ UK; fax: 444(1223)336033; e-mail: deposit@ccdc.cam.ac.uk].
  • 26
    • 33845551193 scopus 로고
    • (a) In all cases only one isomer was observed in the NMR spectrum (after removal of the Boc group) or by HPLC. Reductive amination of cyclic ketones in these conditions is usually not selective: Hutchins, R. O.; Su, W.-Y.; Sivakumar, R.; Cistone, F.; Stercho, Y. P. J. Org. Chem. 1983, 48, 3412.
    • (1983) J. Org. Chem. , vol.48 , pp. 3412
    • Hutchins, R.O.1    Su, W.-Y.2    Sivakumar, R.3    Cistone, F.4    Stercho, Y.P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.