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Volumn 44, Issue 5, 2003, Pages 937-940

An easy and stereoselective synthesis of N-Boc-dolaproine via the Baylis-Hillman reaction

Author keywords

Amino aldehydes; Baylis Hillman; Dolaproine; Hydrogenation

Indexed keywords

AMINO ACID DERIVATIVE; ANTINEOPLASTIC AGENT; DOLASTATIN 10; N TERT BUTYLOXYCARBONYL DOLAPROLINE; PENTAPEPTIDE; UNCLASSIFIED DRUG;

EID: 0037467814     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02765-X     Document Type: Article
Times cited : (56)

References (61)
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    • 27=-54.5° (c 1, MeOH)
    • 27=-54.5° (c 1, MeOH).
  • 59
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    • 3), 3.16 (m, 1H), 2.47 (m, 1H), 1.96-1.82 (m, 4H), 1.72 (m, 1H), 1.44 (s, 9H), 1.18 (d, 3H, J=7 Hz)
    • 3), 3.16 (m, 1H), 2.47 (m, 1H), 1.96-1.82 (m, 4H), 1.72 (m, 1H), 1.44 (s, 9H), 1.18 (d, 3H, J=7 Hz).
  • 60
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    • For an example of a Baylis-Hillman reaction with 4-oxoazetidine-carboaldehydes without racemization, see: and references cited therein
    • For an example of a Baylis-Hillman reaction with 4-oxoazetidine-carboaldehydes without racemization, see: Alcaide B., Almendros P., Aragoncillo C. J. Org. Chem. 66:2001;1612-1620. and references cited therein.
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    • Alcaide, B.1    Almendros, P.2    Aragoncillo, C.3
  • 61
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    • For an example of a Baylis-Hillman reaction using a configurational restricted amino aldehyde without racemization, see:
    • For an example of a Baylis-Hillman reaction using a configurational restricted amino aldehyde without racemization, see: Nayak S.K., Thijs L., Zwanenburg B. Tetrahedron Lett. 40:1999;981-984.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 981-984
    • Nayak, S.K.1    Thijs, L.2    Zwanenburg, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.