Brevisamide: an unprecedented monocyclic ether alkaloid from the dinoflagellate Karenia brevis that provides a potential model for ladder-frame initiation.
about
An asymmetric total synthesis of brevisamideDevelopment of a fluorescence assay for the characterization of brevenal binding to rat brain synaptosomes.Electrophilic and nucleophilic enzymatic cascade reactions in biosynthesis.Review of Florida Red Tide and Human Health Effects.A Formal Total Synthesis of (-)-Brevisamide.A concise asymmetric total synthesis of (+)-brevisamide.Brevenal, a brevetoxin antagonist from Karenia brevis, binds to a previously unreported site on mammalian sodium channelsThe development of endo-selective epoxide-opening cascades in water.Synthesis of marine polycyclic polyethers via endo-selective epoxide-opening cascadesBiosynthesis and molecular genetics of polyketides in marine dinoflagellates.SmI2-induced cyclizations and their applications in natural product synthesis.Microalgae in the postgenomic era: a blooming reservoir for new natural products.Polyketide biosynthesis in dinoflagellates: what makes it different?Total synthesis of brevisamide.Characterization of tamulamides A and B, polyethers isolated from the marine dinoflagellate Karenia brevis.Total synthesis of (-)-brevisin: a concise synthesis of a new marine polycyclic ether.Absolute configuration of brevisamide and brevisin: confirmation of a universal biosynthetic process for Karenia brevis polyethers.Achmatowicz Reaction and its Application in the Syntheses of Bioactive Molecules.Intramolecular hydroalkoxylation of non-activated C=C bonds catalysed by zeolites: an experimental and theoretical study.Enantioselective synthesis of δ-/γ-alkoxy-β-hydroxy-α-alkyl-substituted Weinreb amides via DKR-ATH: application to the synthesis of advanced intermediate of (-)-brevisamide.The Negishi Cross-Coupling in the Synthesis of Natural Products and Bioactive Molecules
P2860
Q24655897-D85DC62E-F675-4E3B-92C3-A76BDF6471A3Q34249768-DEB7BB1B-47A4-4439-815E-36F906658066Q34252286-A4AC3672-31A8-4F16-BFC2-9860D39B3928Q34460142-3643C515-7225-41D2-AD97-04C188163979Q34974293-0ABFA528-5902-4114-9A15-3535B019F496Q36002403-D6A7C3D2-98A4-4865-80F8-1F05D52A854CQ36933968-7B902808-FE01-419D-ADF0-B5C121FF39E8Q37619274-FC0E37FD-344F-47EE-986A-664BF6ECF6F8Q37735711-2954D2AC-DBD7-468C-9E9F-FE731CD632E1Q37755983-8D7D5318-A1FC-4256-8ACA-8C928B750A2CQ37760869-56C276ED-0485-4B23-B028-0078EC9A719EQ37957116-8DFA60A6-D2B6-4712-B25F-05F8E747E4E4Q38220326-5C9531B5-2416-4009-971F-D6C6EB9DBBABQ39613564-A84BD2CD-FE9D-43B9-A54B-848FCA4E880CQ40906164-B462BD04-C130-4804-82A6-A7335217EC71Q41763562-247217B4-71EF-4137-B82E-59A06C44675FQ41876157-227D8270-8283-40F1-A7AC-04B8210E4E69Q44167873-8F6CC4A0-902F-4CF6-8FED-20D6F5A62D47Q45972879-C5723BB9-9349-4D42-92A5-CD904E9B648FQ51787642-4E2C7943-B78C-4314-AC66-ED5E6DB806B3Q58101062-9C4B0B46-5B7B-40BC-992A-B8A9D118A30C
P2860
Brevisamide: an unprecedented monocyclic ether alkaloid from the dinoflagellate Karenia brevis that provides a potential model for ladder-frame initiation.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Brevisamide: an unprecedented ...... l for ladder-frame initiation.
@en
Brevisamide: an unprecedented ...... l for ladder-frame initiation.
@nl
type
label
Brevisamide: an unprecedented ...... l for ladder-frame initiation.
@en
Brevisamide: an unprecedented ...... l for ladder-frame initiation.
@nl
prefLabel
Brevisamide: an unprecedented ...... l for ladder-frame initiation.
@en
Brevisamide: an unprecedented ...... l for ladder-frame initiation.
@nl
P2093
P2860
P356
P1433
P1476
Brevisamide: an unprecedented ...... l for ladder-frame initiation.
@en
P2093
Andrea J Bourdelais
Daniel G Baden
Jeffrey L C Wright
Masayuki Satake
Ryan M Van Wagoner
P2860
P304
P356
10.1021/OL801243N
P407
P577
2008-07-23T00:00:00Z