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22
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67549106317
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note
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This sponge was originally described as Eurypon laughlini.
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23
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67549084083
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note
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8, 827.4456).
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24
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67549147783
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note
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2 gas.
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26
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0027973157
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5 as the solvent (see Ref. 12). Slowly interconverting conformations have been observed in other cyclic peptides such as schizotrin A and pahayokolides; see
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5 as the solvent (see Ref. 12). Slowly interconverting conformations have been observed in other cyclic peptides such as schizotrin A and pahayokolides; see. Pergament I., and Carmeli S. Tetrahedron Lett. 35 (1994) 8473-8476
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Pergament, I.1
Carmeli, S.2
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27
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34250703208
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An T., Krishnaswamy T., Kumar S., Wang M., Liu L., Lay J.O., Liyanage R., Berry J., Gantar M., Marks V., Gawley R.E., and Rein K.S. J. Nat. Prod. 70 (2007) 730-735
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An, T.1
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Lay, J.O.6
Liyanage, R.7
Berry, J.8
Gantar, M.9
Marks, V.10
Gawley, R.E.11
Rein, K.S.12
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28
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67549085822
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note
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2 = 0.1418 for 541 variable parameters, GOF = 1.034. The crystallographic data for euryjanicin A (1) have been deposited at CCDC under the registry number 721666. They can be obtained free of charge at www.ccdc.cam.ac.uk/conts/retrieving.html [or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge, CB2 1EZ, UK; fax: +44 1223 336033; e-mail: deposit@ccdc.cam.ac.uk].
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30
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0033573120
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Renner M.K., Shen Y.-C., Cheng X.-C., Jensen P.R., Frankmoelle W., Kauffman C.A., Fenical W., Labbovsky E., and Clardy J. J. Am. Chem. Soc. 121 (1999) 11273-11276
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Jensen, P.R.4
Frankmoelle, W.5
Kauffman, C.A.6
Fenical, W.7
Labbovsky, E.8
Clardy, J.9
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