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Volumn 125, Issue 40, 2003, Pages 12172-12178

Asymmetric, stereocontrolled total synthesis of paraherquamide A

Author keywords

[No Author keywords available]

Indexed keywords

ENANTIOSELECTIVITY;

EID: 0141992307     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja036713+     Document Type: Article
Times cited : (96)

References (77)
  • 42
    • 0141974483 scopus 로고    scopus 로고
    • U.S. Patent 5,750,695, 1998
    • (g) Lee, B. H.; Clothier, M. F. U.S. Patent 5,750,695, 1998.
    • Lee, B.H.1    Clothier, M.F.2
  • 64
    • 0029906967 scopus 로고    scopus 로고
    • Since this route was developed, McWhorter and Savall have published a route to 45 which is shorter and higher yielding, but the applicability of their synthesis on a large scale has not yet been demonstrated. Savall, B. M.; McWhorter, W. W. J. Org. Chem. 1996, 61, 8696-8697.
    • (1996) J. Org. Chem. , vol.61 , pp. 8696-8697
    • Savall, B.M.1    McWhorter, W.W.2
  • 68
    • 0141905418 scopus 로고    scopus 로고
    • note
    • 1H NMR data. In compounds where the indole substituent is on the same face of the diketopiperazine as the MOM ether, the signal for the methoxy group is at significantly higher field than in the situation where these two substituents are on opposite faces. This is due to the proximity of the methoxy group to the shielding effects of the aromatic system.
  • 70
    • 0142009147 scopus 로고    scopus 로고
    • note
    • The synlanti relationship in this case refers to the relative stereochemistry between the C-20 stereogenic center (see paraherquamide numbering) and the proline residue. Equation Presented


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.