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Journal articles on the topic 'Ulapualide A'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Allingham, John S., Junichi Tanaka, Gerard Marriott, and Ivan Rayment. "Absolute Stereochemistry of Ulapualide A." Organic Letters 6, no. 4 (February 2004): 597–99. http://dx.doi.org/10.1021/ol036458y.

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2

Celatka, Cassandra A., and James S. Panek. "Asymmetric synthesis of a C1C19 fragment of ulapualide A." Tetrahedron Letters 43, no. 39 (September 2002): 7043–46. http://dx.doi.org/10.1016/s0040-4039(02)01553-8.

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3

Roesener, Jeffrey A., and Paul J. Scheuer. "Ulapualide A and B, extraordinary antitumor macrolides from nudibranch eggmasses." Journal of the American Chemical Society 108, no. 4 (February 1986): 846–47. http://dx.doi.org/10.1021/ja00264a052.

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4

Vincent, E., J. Saxton, C. Baker-Glenn, I. Moal, J. D. Hirst, G. Pattenden, and P. E. Shaw. "Effects of ulapualide A and synthetic macrolide analogues on actin dynamics and gene regulation." Cellular and Molecular Life Sciences 64, no. 4 (February 2007): 487–97. http://dx.doi.org/10.1007/s00018-007-6427-1.

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5

Chattopadhyay, Shital K., James Kempson, Alan McNeil, Gerald Pattenden, Michael Reader, David E. Rippon, and David Waite. "Towards a total synthesis of ulapualide A. Concise synthetic routes to the tris-oxazole ring system and tris-oxazole macrolide core in ulapualides, kabiramides, halichondramides, mycalolides and halishigamides." Journal of the Chemical Society, Perkin Transactions 1, no. 15 (2000): 2415–28. http://dx.doi.org/10.1039/b000750l.

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6

Panek, James S., Richard T. Beresis, and Cassandra A. Celatka. "Studies Directed toward the Synthesis of Ulapualide A. Asymmetric Synthesis of the C26−C42 Fragment." Journal of Organic Chemistry 61, no. 19 (January 1996): 6494–95. http://dx.doi.org/10.1021/jo960531z.

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7

Pattenden, Gerald, Neil J Ashweek, Charles A G. Baker-Glenn, Gary M Walker, and James G K. Yee. "Total Synthesis of (−)-Ulapualide A: The Danger of Overdependence on NMR Spectroscopy in Assignment of Stereochemistry." Angewandte Chemie International Edition 46, no. 23 (June 4, 2007): 4359–63. http://dx.doi.org/10.1002/anie.200700459.

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8

Pattenden, Gerald, Neil J Ashweek, Charles A G. Baker-Glenn, Gary M Walker, and James G K. Yee. "Total Synthesis of (−)-Ulapualide A: The Danger of Overdependence on NMR Spectroscopy in Assignment of Stereochemistry." Angewandte Chemie 119, no. 23 (June 4, 2007): 4437–41. http://dx.doi.org/10.1002/ange.200700459.

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9

Chattopadhyay, Shital, and Gerald Pattenden. "A Convergent Synthesis of the tris-Oxazole Ring System in Ulapualide A and Related Marine Metabolites." Synlett 12, no. 12 (December 31, 2000): 1342–44. http://dx.doi.org/10.1055/s-1997-1056.

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10

Chattopadhyay, Shital K., James Kempson, Alan McNeil, Gerald Pattenden, Michael Reader, David E. Rippon, and David Waite. "ChemInform Abstract: Towards a Total Synthesis of Ulapualide A. Concise Synthetic Routes to the tris-Oxazole Ring System (XI) and tris-Oxazole Macrolide Core (XVII) in Ulapualides, Kabiramides, Halichondramides, Mycalolides, and Halishigamides." ChemInform 31, no. 48 (November 28, 2000): no. http://dx.doi.org/10.1002/chin.200048221.

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11

Chattopadhyay, Shital K., and Gerald Pattenden. "Total synthesis of ulapualide A, a novel tris-oxazole containing macrolide from the marine nudibranch Hexabranchus sanguineus." Tetrahedron Letters 39, no. 33 (August 1998): 6095–98. http://dx.doi.org/10.1016/s0040-4039(98)01257-x.

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12

PANEK, J. S., R. T. BERESIS, and C. A. CELATKA. "ChemInform Abstract: Studies Directed Toward the Synthesis of Ulapualide A. Asymmetric Synthesis of the C26-C42 Fragment." ChemInform 28, no. 6 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199706221.

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13

Panek, James S., and Richard T. Beresis. "Studies Directed toward the Synthesis of Ulapualide A. Asymmetric Synthesis of the C8−C25 Tris-Oxazole Fragment." Journal of Organic Chemistry 61, no. 19 (January 1996): 6496–97. http://dx.doi.org/10.1021/jo960532r.

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14

CHATTOPADHYAY, S. K., and G. PATTENDEN. "ChemInform Abstract: A Convergent Synthesis of the tris-Oxazole Ring System in Ulapualide A and Related Marine Metabolites." ChemInform 29, no. 13 (June 23, 2010): no. http://dx.doi.org/10.1002/chin.199813231.

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15

Pattenden, Gerald, Neil J. Ashweek, Charles A. G. Baker-Glenn, James Kempson, Gary M. Walker, and James G. K. Yee. "Total synthesis of (−)-ulapualide A, a novel tris-oxazole macrolide from marine nudibranchs, based on some biosynthesis speculation." Organic & Biomolecular Chemistry 6, no. 8 (2008): 1478. http://dx.doi.org/10.1039/b801036f.

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16

Chattopadhyay, Shital K., and Gerald Pattenden. "A total synthesis of the unique tris-oxazole macrolide ulapualide A produced by the marine nudibranch Hexabranchus sanguineus." Journal of the Chemical Society, Perkin Transactions 1, no. 15 (2000): 2429–54. http://dx.doi.org/10.1039/b000751j.

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17

Celatka, Cassandra A., Ping Liu, and James S. Panek. "Studies directed toward the synthesis of ulapualide A: Phosphorus-based olefination as model studies for (Schlosser-like) fragment coupling." Tetrahedron Letters 38, no. 31 (August 1997): 5449–52. http://dx.doi.org/10.1016/s0040-4039(97)01219-7.

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18

PANEK, J. S., and R. T. BERESIS. "ChemInform Abstract: Studies Directed Toward the Synthesis of Ulapualide A. Asymmetric Synthesis of the C8-C25 Tris-Oxazole Fragment." ChemInform 28, no. 6 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199706222.

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19

CHATTOPADHYAY, S. K., and G. PATTENDEN. "ChemInform Abstract: Total Synthesis of Ulapualide A, a Novel tris-Oxazole Containing Macrolide from the Marine Nudibranch Hexabranchus sanguineus." ChemInform 29, no. 44 (June 19, 2010): no. http://dx.doi.org/10.1002/chin.199844263.

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20

Chattopadhyay, Shital K., and Gerald Pattenden. "ChemInform Abstract: A Total Synthesis of the Unique Tris-Oxazole Macrolide Ulapualide A Produced by the Marine Nudibranch Hexabranchus sanguineus." ChemInform 31, no. 48 (November 28, 2000): no. http://dx.doi.org/10.1002/chin.200048222.

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21

Chattopadhyay, Shital, and Gerald Pattenden. "Towards a Total Synthesis of Ulapualide A. A Concise Synthesis of the tris-Oxazole Macrolide Core and Entire Carbon Skeleton." Synlett 12, no. 12 (December 31, 2000): 1345–48. http://dx.doi.org/10.1055/s-1997-1055.

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22

CELATKA, C. A., P. LIU, and J. S. PANEK. "ChemInform Abstract: Studies Directed Toward the Synthesis of Ulapualide A: Phosphorus- Based Olefination as Model Studies for (Schlosser-Like) Fragment Coupling." ChemInform 28, no. 44 (August 3, 2010): no. http://dx.doi.org/10.1002/chin.199744278.

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23

Chattopadhyay, Shital K., and Gerald Pattenden. "Synthetic studies towards novel tris-oxazole based macrolides of marine origin. Stereocontrolled synthesis of the C20C35 fragment in ulapualide A." Tetrahedron Letters 36, no. 29 (July 1995): 5271–74. http://dx.doi.org/10.1016/0040-4039(95)00955-c.

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24

Chattopadhyay, S. "Synthetic Studies towards Novel tris-Oxazole based Macrolides of Marine Origin. Stereocontrolled Synthesis of the C20-C35 Fragment in Ulapualide A." Tetrahedron Letters 36, no. 29 (July 17, 1995): 5271–74. http://dx.doi.org/10.1016/00404-0399(50)0955c-.

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25

CHATTOPADHYAY, S. K., and G. PATTENDEN. "ChemInform Abstract: Towards a Total Synthesis of Ulapualide A. A Concise Synthesis of the tris-Oxazole Macrolide Core and Entire Carbon Skeleton." ChemInform 29, no. 13 (June 23, 2010): no. http://dx.doi.org/10.1002/chin.199813232.

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26

CHATTOPADHYAY, S. K., and G. PATTENDEN. "ChemInform Abstract: Synthetic Studies Towards Novel tris-Oxazole Based Macrolides of Marine Origin. Stereocontrolled Synhesis of the C20-C35 Fragment (I) in Ulapualide A." ChemInform 26, no. 43 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199543272.

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27

Knight, David W., Gerald Pattenden, and David E. Rippon. "Synthesis of the Tris-oxazole Ring System of Ulapualides." Synlett 1990, no. 01 (1990): 36–37. http://dx.doi.org/10.1055/s-1990-20977.

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28

Parrish, Stephen M., Wesley Yoshida, Baojun Yang, and Philip G. Williams. "Ulapualides C–E Isolated from a Hawaiian Hexabranchus sanguineus Egg Mass." Journal of Natural Products 80, no. 3 (January 18, 2017): 726–30. http://dx.doi.org/10.1021/acs.jnatprod.6b00896.

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29

Fusetani, N., K. Yasumuro, S. Matsunaga, and K. Hashimoto. "Mycalolides A – C, hybrid macrolides of ulapualides and halichondramide, from a sponge of the genus." Tetrahedron Letters 30, no. 21 (January 1989): 2809–12. http://dx.doi.org/10.1016/s0040-4039(00)99131-7.

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30

Kempson, James, and Gerald Pattenden. "A Macrolactamisation-Oxazoline Ring Forming Approach towards the tris-Oxazole Macrolide Core in the Ulapualides." Synlett 1999, no. 5 (May 1999): 533–36. http://dx.doi.org/10.1055/s-1999-2671.

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31

Kempson, James, and Gerald Pattenden. "ChemInform Abstract: A Macrolactamization-Oxazoline Ring Forming Approach Towards the Tris-oxazole Macrolide Core in the Ulapualides." ChemInform 30, no. 33 (June 14, 2010): no. http://dx.doi.org/10.1002/chin.199933285.

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32

Maddock, John, Gerald Pattenden, and Paul G. Wight. "Stereochemistry of ulapualides, a new family of tris-oxazole-containing macrolide ionophores from marine nudibranchs. A molecular mechanics study." Journal of Computer-Aided Molecular Design 7, no. 5 (October 1993): 573–86. http://dx.doi.org/10.1007/bf00124363.

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33

"Synthesis of (-)-Ulapualide A." Synfacts 2008, no. 08 (July 23, 2008): 0784. http://dx.doi.org/10.1055/s-2008-1078536.

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34

Allingham, John S., Junichi Tanaka, Gerard Marriott, and Ivan Rayment. "Absolute Stereochemistry of Ulapualide A." ChemInform 35, no. 26 (June 29, 2004). http://dx.doi.org/10.1002/chin.200426189.

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35

Celatka, Cassandra A., and James S. Panek. "Asymmetric Synthesis of a C1—C19 Fragment of Ulapualide A." ChemInform 34, no. 2 (January 14, 2003). http://dx.doi.org/10.1002/chin.200302210.

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36

ROESENER, J. A., and P. J. SCHEUER. "ChemInform Abstract: Ulapualide A (Ia) and B (Ib), Extraordinary Antitumor Macrolides from Nudibranch Eggmasses." Chemischer Informationsdienst 17, no. 25 (June 24, 1986). http://dx.doi.org/10.1002/chin.198625327.

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37

Pattenden, Gerald, Neil J. Ashweek, Charles A. G. Baker-Glenn, Gary M. Walker, and James G. K. Yee. "Total Synthesis of (-)-Ulapualide A (I): The Danger of Overdependence on NMR Spectroscopy in Assignment of Stereochemistry." ChemInform 38, no. 40 (October 2, 2007). http://dx.doi.org/10.1002/chin.200740198.

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38

Pattenden, Gerald, Neil J. Ashweek, Charles A. G. Baker-Glenn, James Kempson, Gary M. Walker, and James G. K. Yee. "ChemInform Abstract: Total Synthesis of (-)-Ulapualide A, a Novel tris-Oxazole Macrolide from Marine Nudibranchs, Based on Some Biosynthesis Speculation." ChemInform 39, no. 35 (August 26, 2008). http://dx.doi.org/10.1002/chin.200835203.

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39

KNIGHT, D. W., G. PATTENDEN, and D. E. RIPPON. "ChemInform Abstract: Synthesis of the Trisoxazole Ring System of Ulapualides." ChemInform 21, no. 22 (May 29, 1990). http://dx.doi.org/10.1002/chin.199022151.

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