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References from Total Synthesis of Marine Alkaloids Motuporamines A and B via Ring Expansion of Cyclic β-Keto Esters. Local targets link to admitted publications; unresolved targets remain external evidence.
Cancer control potential of marine natural product scaffolds through inhibition of tumor cell migration and invasion
10.1016/j.drudis.2016.06.032 · 2016 · External reference
Marine-Derived Macrocyclic Alkaloids (MDMAs): Chemical and Biological Diversity
10.3390/md18070368 · 2020 · External reference
Motuporamines A–C, Cytotoxic Alkaloids Isolated from the Marine Sponge Xestospongia exigua (Kirkpatrick)
10.1021/jo980355p · 1998 · External reference
Motuporamines, Anti-Invasion and Anti-Angiogenic Alkaloids from the Marine Sponge Xestospongia exigua (Kirkpatrick): Isolation, Structure Elucidation, Analogue Synthesis, and Conformational Analysis
10.1021/jo016101c · 2002 · External reference
Motuporamine Derivatives as Antimicrobial Agents and Antibiotic Enhancers against Resistant Gram-Negative Bacteria
10.1002/cbic.201600532 · 2017 · External reference
The Tumor Invasion Inhibitor Dihydromotuporamine C Activates RHO, Remodels Stress Fibers and Focal Adhesions, and Stimulates Sodium-Proton Exchange
10.1158/0008-5472.can-03-2733 · 2004 · External reference
Inhibition of Tumor Cell Invasion and Angiogenesis by Motuporamines
2001 · External reference
Total synthesis of cytotoxic sponge alkaloids motuporamines A and B
10.1016/s0040-4039(99)01016-3 · 1999 · External reference
Cytotoxic Alkaloids Motuporamines A–C: Synthesis and Structural Verification
10.1021/ol991029e · 1999 · External reference
Synthesis of Oxygen- and Nitrogen-Containing Heterocycles by Ring-Closing Metathesis
10.1021/cr0200872 · 2004 · External reference
Tandem Conjugate Additions and 3-Aza-Cope Rearrangements of Tertiary Allyl Amines and Cyclic α-Vinylamines with Acetylenic Sulfones. Applications to Simple and Iterative Ring Expansions Leading to Medium and Large-Ring Nitrogen Heterocycles
10.1021/jo800600a · 2008 · External reference
Tandem Nucleophilic Addition/Oxy-2-azonia-Cope Rearrangement for the Formation of Homoallylic Amides and Lactams: Total Synthesis and Structural Verification of Motuporamine G
10.1021/ja310002m · 2012 · External reference
Irreversible Oxy-2-azonia-Cope Rearrangements for the Synthesis of Functionalized Allyl α-Amino Acid Derivatives
10.1002/ejoc.201301818 · 2014 · External reference
The Synthesis of Structurally Diverse Macrocycles By Successive Ring Expansion
10.1002/anie.201509153 · 2015 · External reference
Ring-Expansion Approach to Medium-Sized Lactams and Analysis of Their Medicinal Lead-Like Properties
10.1002/chem.201605615 · 2017 · External reference
Consecutive Ring-Expansion Reactions for the Iterative Assembly of Medium-Sized Rings and Macrocycles
10.1055/s-0037-1611500 · 2020 · External reference
Synthesis of Cyclic Peptide Mimetics by the Successive Ring Expansion of Lactams
10.1002/chem.201703316 · 2017 · External reference
Procedures for the acylation of diethyl malonate and ethyl acetoacetate with acid chlorides using tertiary amine bases and magnesium chloride
10.1021/jo00215a003 · 1985 · External reference
The 9-fluorenylmethyloxycarbonyl family of base-sensitive amino-protecting groups
10.1021/ar00143a003 · 1987 · External reference
Tris(2-aminoethyl)amine as substitute for 4-(aminomethyl)piperidine in the FMOC/polyamine approach to rapid peptide synthesis
10.1021/jo00292a050 · 1990 · External reference
Ring-Closing Alkyne Metathesis. Stereoselective Synthesis of the Cytotoxic Marine Alkaloid Motuporamine C
10.1021/jo991944d · 2000 · External reference
A new synthesis of cyclic allenic esters
10.1021/jo01305a034 · 1980 · External reference
Enamine Chemistry. VI. Reactions with Propiolates
10.1021/jo01027a011 · 1963 · External reference
Unresolved reference
2003 · External reference
