메뉴 건너뛰기




Volumn 40, Issue 42, 1999, Pages 7441-7444

Synthesis of the tripeptide (C1-N12) and hydroxylated hexadecene (C26-C41) domains of sanglifehrin A and C

Author keywords

Aldols; Aminal; Immunosuppressive compounds; Peptide; Stereocontrol

Indexed keywords

ALDEHYDE; AMINO ACID DERIVATIVE; HEXADECENE; IMMUNOSUPPRESSIVE AGENT; SANGLIFEHRIN A; SANGLIFEHRIN C; TRIPEPTIDE; UNCLASSIFIED DRUG;

EID: 0033570293     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)01539-7     Document Type: Article
Times cited : (20)

References (21)
  • 1
    • 0009748665 scopus 로고    scopus 로고
    • Intern. Patent Appl. W097/02285 (January 23, 1997)
    • (a) Fehr, T.; Oberer, L. Intern. Patent Appl. W097/02285 (January 23, 1997). (b) Fehr, T.; Oberer, L.; Quesniaux, R. V.; Sanglier, J.-J.; Schuler, W.; Sedrani, R. Intern. Patent Appl. W098/07743 (March 3, 1998).
    • Fehr, T.1    Oberer, L.2
  • 3
    • 0009733539 scopus 로고    scopus 로고
    • The affinity of 1 for cyclophilin A is 20-fold greater than that exhibited by cyclosporin A
    • The affinity of 1 for cyclophilin A is 20-fold greater than that exhibited by cyclosporin A.
  • 12
    • 0027050190 scopus 로고
    • The formation of an inseparable by-product (N-pivaloyloxazolidinone) was observed if the same reaction was carried out under the conditions described by Evans
    • The formation of an inseparable by-product (N-pivaloyloxazolidinone) was observed if the same reaction was carried out under the conditions described by Evans (Evans, D. A.; Gage, J. R.; Leighton, J. L. J. Am. Chem. Soc. 1992, 114, 9434).
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 9434
    • Evans, D.A.1    Gage, J.R.2    Leighton, J.L.3
  • 13
    • 0026703867 scopus 로고
    • (a) Paterson, I.; Tillyer, R. D. Tetrahedron Lett. 1992, 33, 4233. (b) Paterson, I.; Norcross, R. D.; Ward, R. A.; Romea, P.; Lister, M. A. J. Am. Chem. Soc. 1994, 116, 11287.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 4233
    • Paterson, I.1    Tillyer, R.D.2
  • 17
    • 0009733166 scopus 로고    scopus 로고
    • The previously unknown ketone 17 was prepared by acylation of (S)-4-benzyl-2-oxazolidinone with 5-hexenoic acid, enantiocontrolled α-methylation of the amide, formation of the Weinreb amide, and condensation of the latter with methyllithium
    • The previously unknown ketone 17 was prepared by acylation of (S)-4-benzyl-2-oxazolidinone with 5-hexenoic acid, enantiocontrolled α-methylation of the amide, formation of the Weinreb amide, and condensation of the latter with methyllithium.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.