Uypnonc


T. Uibanski, Chemistry and Technology of Explosives, Vol. 3, Peigamon Press, Inc., New York, 1967.  [c.56]

Feeding experiments utilizing C-, N-, and H-labeled cadaverine (44) and lysine (24) in l upinus augustifolius a source of the lupine alkaloids (—)-sparteine (50, R = H,H) and (+)-lupanine (50, R = O), have been reported which lend dramatic credence to the entire biosynthetic sequence for these and the related compounds discussed above (41). That is, the derivation of these bases is in concert with the expected cyclization from the favored aH-trans stereoisomer of the trimer expected on self-condensation of the 1-dehydropiperidine (45).  [c.539]

W. Biemacki and T. Uibanski, Bull. Acad. Polon. Sci., Ser. Sci. Chem. 10, 601 (1962).  [c.105]

Ubenimex, [(2(3),3(R))-3-amino-2-hydroxy-4-phenylbutanoyl]-L-leucine, was isolated as an inhibitor of aminopeptidases, on which it acts as a strong, reversible transition-state analogue inhibitor (293). Analogues of ubenimex have been made and some other aminopeptidase inhibitors, not all of them peptides, have been isolated from streptomycetes (294—296).  [c.159]

T. Uebanski, Departmei]t of Organic Technology, Institute of Tech-  [c.463]

Barnett, H. J., and Morse, C. (1963). Scarcity and Growth The Economics of Natural Resource Availability. Baltimore Johns Hopkins Press for Resources for the Future. Brennan, T. J. Palmer, K. L. Koop, R. J. Ki upmck, A. J. Stagliano, V. and Burtraw, U. (1996). A Shock to the System Restructuring America s Electricity Industry. Washington, DC Resources for the Future.  [c.461]


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Practical organic chemistry (0) -- [ c.210 ]