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Volumn 15, Issue 38, 2009, Pages 9928-9937

Stereocontrolled and versatile total synthesis of bispyrrolidinoindoline diketopiperazine alkaloids: structural revision of the fungal isolate (+)-Asperdimin

Author keywords

Alkaloids; Asperdimin; Bispyrrolidinoindolines; Dimerization; Heterodimers

Indexed keywords

ABSOLUTE CONFIGURATION; ASPERDIMIN; BOND FORMATION; DIASTEREOMERS; DIASTEREOSELECTIVE; DIKETOPIPERAZINES; EPIMERIZATION; FUNGAL ISOLATES; HETERODIMERS; NATURAL PRODUCTS; STEREO-SELECTIVE; SYNTHETIC METHODOLOGY; TOTAL SYNTHESIS;

EID: 70450161416     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200901056     Document Type: Article
Times cited : (65)

References (49)
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    • Peptide couplings in similar sterically crowded amino positions have been previously carried out using HATU as coupling agent. See: a) P. R. Hewitt, E. Cleator, S. V. Ley, Org. Biomol. Chem. 2004, 2, 2415-2417;
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    • Unfortunately, we have been unable to obtain a sample or copies of the spectra of the genuine natural product from the Meurer-Grimes laboratory to compare the chromatographic and spectroscopic prop- L erties of the synthetic and natural materials. We thank Dr. Murray Tait for kindly attending to our request.
    • Unfortunately, we have been unable to obtain a sample or copies of the spectra of the genuine natural product from the Meurer-Grimes laboratory to compare the chromatographic and spectroscopic prop- L erties of the synthetic and natural materials. We thank Dr. Murray Tait for kindly attending to our request.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.