Isolation and structure of dolastatin 17

Heterocycles

Volumn 47, Issue 1, 1998, Pages 491-496

  Pettit, George R ^a   Xu, Jun Ping ^a   Hogan, Fiona ^a   Cerny, Ronald L ^a  

^a ARIZONA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001430591     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-97-s(n)8     Document Type: Article

References (14)

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2. b) We are pleased to dedicate this contribution to Dr. Koji Nakanishi in commemoration of his 75th birthday;
3. Midwest Center for Mass Spectrometry, University of Nebraska-Lincoln, Lincoln, Nebraska 68588-0362.
4. G. R. Pettit, J. K. Srirangam, J. Barkóczy, M. D. Williams, M. R. Boyd, E. Hamel, R. Bai, J.-C. Chapuis, and J. M. Schmidt, Anti-Cancer Drug Design, 1996, 10, 529.
5. G. R. Pettit, "The Dolastatins" in Progress in the Chemistry of Organic Natural Products, Vol. 70, Springer-Verlag, Wien-New York, 1997, pp 1-79.
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12. 3CN (9:1) for the 2-hydroxyisovaleric acid; detection at 230.4 and 550 nm. The retention times (min) of the authentic amino and hydroxy acids: L-MeVal (6.794), D-MeVal (10.910), L-Pro (8.612), D-Pro (18.800), L-Leu (39.420), D-Leu (69.891), S-Hiv (12.036) and R-Hiv (19.520).
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