Ahmed, F. et al., “Convergent Synthesis of the C31-C46 Domain of the Phorboxazole Natural Products,” Tetrahedron Letters, vol. 39, pp. 183-186 (1998). |
Carbonetto, S., “The extracellular matrix of the nervous system,” Trends in NeuroSci., pp. 382-387 (Oct. 1984). |
Cink, R. et al., “Stereoselective Synthesis of the C3-C17 Bis-Oxane Domain of Phorboxazole A,” J. Org. Chem., vol. 62, No. 17, pp. 5672-5673 (Aug. 22, 1997). |
Evans, D. et al., “Application of Complex Aldol Reactions to the Total Synthesis of Phorboxazole B,” J. Am. Chem. Soc., vol. 122, No. 41, pp. 10033-10046 (Oct. 18, 2000). |
Forsyth, C. et al., “Total Synthesis of Phorboxazole A”, J. Am. Chem. Soc., vol. 120, No. 22, pp. 5597-5598 (Jun. 10, 1998). |
Knorr, R. et al., “New Coupling Reagents in Peptide Chemistry,” Tetrahedron Lett., vol. 30, No. 15, pp. 1927-1930 (1989). |
Konig, W. et al., “Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid und 3-Hydroxy-4-oxo-3.4-dihydro-1.2.3-benzotriazin,” Chem. Ber., vol. 103, No. 7, pp. 2034-2040 (1970). |
Molinski, T., “Absolute Configuration of Phorboxazoles A and B from the Marine Sponge, Phorbas Sp. 2. C43 and Complete Stereochemistry,” Tetrahedron Letters, vol. 37, No. 44, pp. 7879-7880 (Sep. 4, 1996). |
Paterson, I. et al., “Towards the Total Synthesis of Phorboxazoles A and B: Stereocontrolled Synthesis of a C20-C32 Subunit,” Tetrahedron Letters, vol. 39, pp. 7185-7188 (1998). |
Pattenden, G. et al., “Synthetic Studies Towards Phorboxazole A. A Convergent Synthesis of the C31-C46 Polyene Oxane-Hemiacetal Side Chain,” Tetrahedron Letters, vol. 39, pp. 6099-6102 (1998). |
Rutka, J. et al., “The extracellular matrix of the central and peripheral nervous systems: structure and function,” J. Neurosurg., vol. 69, No. 2, pp. 155-170 (Aug. 1988). |
Searle, P. et al., “Absolute Configuration of Phorboxazoles A and B from the Marine Sponge Phorbas sp. 1. Macrolide and Hemiketal Rings,” J. Am. Chem. Soc., Vol. 118, No. 39, pp. 9422-9423 (Oct. 2, 1996). |
Searle, P. et al., “Phorboxazoles A and B: Potent Cytostatic Macrolides from Marine Sponge Phorbas Sp.,” J. Am. Chem. Soc., vol. 117, No. 31, pp. 8126-8131, (Aug. 9, 1995). |
Uckun, F. et al., “Anticancer Activity of Synthetic Analogues of the Phorboxazoles,” Bioorganic & Medicinal Chemistry Letters, vol. 11, No. 9, pp. 1181-1183 (May 7, 2000). |
Venstrom, K. et al., “Extracellular Matrix 2: Role of extracellular matrix molecules and their receptors in the nervous system,” The FASEB Journal, vol. 7, No. 11, pp. 996-1003 (Aug. 1993). |
Williams, D. et al., “Asymmetric Allylation. An Effective Strategy for the Convergent Synthesis of Highly Functionalized Homoallylic Alcohols,” Tetrahedron Letters, vol. 39, pp. 7251-7254 (1998). |
Wolbers, P. et al., “Structure-Activity Investigations of Analogues of the C15-C26 Phorboxazoles Segment,” Synlett, No. 11, pp. 1808-1810 (Nov. 1999). |
Ye, T. et al., “Synthetic Studies towards Phorboxazole A. A Concise Stereoselective Synthesis of the C20-C26 Pentasubstituted Oxane Ring Unit,” Tetrahedon Letters, vol. 39, pp. 319-322 (1998). |