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Volumn 30, Issue 28, 1989, Pages 3621-3624

Total synthesis of the angiotensin-converting enzyme inhibitor A58365A: On the use of pyroglutamate as a chiral educt

Author keywords

[No Author keywords available]

Indexed keywords

3 CARBOXY 1,2,3,5 TETRAHYDRO 8 HYDROXY 5 OXO 6 INDOLIZIDINEPROPIONIC ACID; UNCLASSIFIED DRUG;

EID: 0024391760     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)80464-0     Document Type: Article
Times cited : (52)

References (18)
  • 6
    • 0001197625 scopus 로고
    • This compound was prepared as described for racemic 4 except starting with L-pyroglutamic acid instead of D,L-pyroglutamic acid
    • (1986) Heterocycles , vol.24 , pp. 2015
    • Nagasaka1    Tsukada2    Hamaguchi3
  • 8
    • 84993854739 scopus 로고
    • Azabicyclic Compounds Synthesis: Reactions of Cyclic β-Enaminoesters with α,β-Unsaturated Carbonyl Compounds
    • For some previous examples of the reaction of vinylogous urethanes with α,β-unsaturated carbonyl compounds leading to pyridone rings see
    • (1985) Synthesis , pp. 735
    • Brunerie1    Celerier2    Huche3    Lhommet4
  • 9
    • 33751173350 scopus 로고
    • Synthesis of 5-Oxoindolizine Derivatives. II: Reaction of Ethyl Pyrrolidin-2-ylideneacetate (an Enamine Ester) with Acyclic a,b-Unsaturated Carbonyl Compounds
    • (1983) HETEROCYCLES , vol.20 , pp. 1099
    • Nagasaka1    Inoue2    Hamaguchi3
  • 15
    • 84918614630 scopus 로고    scopus 로고
    • Compounds 9 and 11 have been derived from A58365A (1) by workers at Eli Lilly & Co. (see ref. 5).
  • 17
    • 84918651170 scopus 로고    scopus 로고
    • 2O, c 0.2) was provided by Dr. Jon. S. Mynderse of Eli Lilly & Co.
  • 18
    • 84918639887 scopus 로고    scopus 로고
    • 2, c 0.9), IR ν [[Truncated]]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.