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Rogers, Evan W., Dalisay, Doralyn S., Molinski, Tadeusz F. (2008) (+)-Zwittermicin A: Assignment of its Complete Configuration by Total Synthesis of the Enantiomer and Implication of D-Serine in its Biosynthesis. Angewandte Chemie, 120 (42). 8206-8209 doi:10.1002/ange.200801561

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Reference TypeJournal (article/letter/editorial)
Title(+)-Zwittermicin A: Assignment of its Complete Configuration by Total Synthesis of the Enantiomer and Implication of D-Serine in its Biosynthesis
JournalAngewandte Chemie
AuthorsRogers, Evan W.Author
Dalisay, Doralyn S.Author
Molinski, Tadeusz F.Author
Year2008 (October 6)Volume120
Issue42
PublisherWiley
DOIdoi:10.1002/ange.200801561Search in ResearchGate
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Mindat Ref. ID7310086Long-form Identifiermindat:1:5:7310086:7
GUID0
Full ReferenceRogers, Evan W., Dalisay, Doralyn S., Molinski, Tadeusz F. (2008) (+)-Zwittermicin A: Assignment of its Complete Configuration by Total Synthesis of the Enantiomer and Implication of D-Serine in its Biosynthesis. Angewandte Chemie, 120 (42). 8206-8209 doi:10.1002/ange.200801561
Plain TextRogers, Evan W., Dalisay, Doralyn S., Molinski, Tadeusz F. (2008) (+)-Zwittermicin A: Assignment of its Complete Configuration by Total Synthesis of the Enantiomer and Implication of D-Serine in its Biosynthesis. Angewandte Chemie, 120 (42). 8206-8209 doi:10.1002/ange.200801561
In(2008, October) Angewandte Chemie Vol. 120 (42) Wiley

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Rogers, Evan W., Dalisay, Doralyn S., Molinski, Tadeusz F. (2008) (+)-Zwittermicin A: Assignment of its Complete Configuration by Total Synthesis of the Enantiomer and Implication of D-Serine in its Biosynthesis. Angewandte Chemie International Edition, 47 (42). 8086-8089 doi:10.1002/anie.200801561
Rogers, Evan W., Molinski, Tadeusz F. (2007) Asymmetric Synthesis of Diastereomeric Diaminoheptanetetraols. A Proposal for the Configuration of (+)-Zwittermicin A. Organic Letters, 9. 437-440 doi:10.1021/ol062804a
Dalisay, Doralyn S., Quach, Tim, Nicholas, Gillian N., Molinski, Tadeusz F. (2009) Amplification of the Cotton Effect of a Single Chromophore through Liposomal Ordering-Stereochemical Assignment of Plakinic Acids I and J. Angewandte Chemie, 121 (24). 4431-4435 doi:10.1002/ange.200900888
Skepper, Colin K., Dalisay, Doralyn S., Molinski, Tadeusz F. (2008) Synthesis and Antifungal Activity of (−)-(Z)-Dysidazirine. Organic Letters, 10. 5269-5271 doi:10.1021/ol802065d
Dalisay, Doralyn S., Rogers, Evan W., Edison, Arthur S., Molinski, Tadeusz F. (2009) Structure Elucidation at the Nanomole Scale. 1. Trisoxazole Macrolides and Thiazole-Containing Cyclic Peptides from the NudibranchHexabranchus sanguineus. Journal of Natural Products, 72. 732-738 doi:10.1021/np8007649
Dalisay, Doralyn S., Quach, Tim, Nicholas, Gillian N., Molinski, Tadeusz F. (2009) Amplification of the Cotton Effect of a Single Chromophore through Liposomal Ordering-Stereochemical Assignment of Plakinic Acids I and J. Angewandte Chemie International Edition, 48 (24). 4367-4371 doi:10.1002/anie.200900888
Dalisay, Doralyn S., Quach, Tim, Molinski, Tadeusz F. (2011) Liposomal Circular Dichroism. Assignment of Remote Stereocenters in Plakinic Acids K and L from aPlakortis–XestospongiaSponge Association. Organic Letters, 13. 4152 doi:10.1021/ol2017752
Dalisay, Doralyn S., Quach, Tim, Molinski, Tadeusz F. (2010) Liposomal Circular Dichroism. Assignment of Remote Stereocenters in Plakinic Acids K and L from aPlakortis−XestospongiaSponge Association. Organic Letters, 12. 1524-1527 doi:10.1021/ol100249v
Dalisay, Doralyn S., Tsukamoto, Sachiko, Molinski, Tadeusz F. (2009) Absolute Configuration of the α,ω-Bifunctionalized Sphingolipid Leucettamol A fromLeucetta microrhaphisby Deconvoluted Exciton Coupled CD⊥. Journal of Natural Products, 72. 353-359 doi:10.1021/np800549n
Dalisay, Doralyn S., Molinski, Tadeusz F. (2009) NMR Quantitation of Natural Products at the Nanomole Scale. Journal of Natural Products, 72. 739-744 doi:10.1021/np900009b
Liu, Chaomin, Masuno, Makoto N., MacMillan, John B., Molinski, Tadeusz F. (2004) Enantioselective Total Synthesis of (+)-Milnamide A and Evidence of Its Autoxidation to (+)-Milnamide D. Angewandte Chemie, 116 (44). 6077-6080 doi:10.1002/ange.200461245
 
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