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Dysidazirine, a cytotoxic azacyclopropene from the marine sponge Dysidea fragilis
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An Azirine Solid-State Photodegradant of the Ccr2/Ccr5 Dual Antagonist Bms-813160
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ChemInform Abstract: Dysidazirine, a Cytotoxic Azacyclopropene from the Marine Sponge Dysidea fragilis.
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inferred← citeshttps://doi.org/10.1016/0742-8413(90)90012-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-13583-5.00008-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00043-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bmcl.2010.01.068openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bse.2007.09.008openalex-snapshot
Chemical variability within the marine sponge Aplysina fulva
inferred← citeshttps://doi.org/10.1016/j.ejmech.2009.05.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jscs.2024.101831openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2018.05.033openalex-snapshot
Facile construction of trifluoromethyl-azirines via one-pot metal-free Neber reaction
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.09.061openalex-snapshot
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Stable but chimeric antiaromatic 1H-azirines? A threefold reinvestigation
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.154164openalex-snapshot
An azirine solid-state photodegradant of the CCR2/CCR5 dual antagonist BMS-813160
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)81296-5openalex-snapshot
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Chapter 2 Marine Alkaloids II
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Absolute configuration of α-phthalimido carboxylic acid derivatives from circular dichroism spectra
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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01286openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.4c01870openalex-snapshot
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Synthesis of 2H-Azirines via Iodine-Mediated Oxidative Cyclization of Enamines
inferred← citeshttps://doi.org/10.1021/acs.jpcb.4c03411openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja300552copenalex-snapshot
Expedient Synthesis of Highly Substituted Pyrroles via Tandem Rearrangement of α-Diazo Oxime Ethers
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inferred← citeshttps://doi.org/10.1021/jo011157sopenalex-snapshot
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The Neber Approach to 2-(Tetrazol-5-yl)-2H-Azirines
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inferred← citeshttps://doi.org/10.1021/jo970581jopenalex-snapshot
Enhancement of the Enantioselectivity in Lipase-Catalyzed Kinetic Resolutions of 3-Phenyl-2H-azirine-2-methanol by Lowering the Temperature to −40 °C
inferred← citeshttps://doi.org/10.1021/jo991389fopenalex-snapshot
Asymmetric Synthesis of 2H-Azirine 2-Carboxylate Esters
inferred← citeshttps://doi.org/10.1021/jp511208popenalex-snapshot
Mechanistic Insight into Decomposition of 2H-Azirines: Electronic Structure Calculations and Dynamics Simulations
inferred← citeshttps://doi.org/10.1021/np300744yopenalex-snapshot
Halisphingosines A and B, Modified Sphingoid Bases from Haliclona tubifera. Assignment of Configuration by Circular Dichroism and van’t Hoff’s Principle of Optical Superposition
inferred← citeshttps://doi.org/10.1021/ol100703ropenalex-snapshot
2H-Azirines from a Concerted Addition of Alkylcarbenes to Nitrile Groups
inferred← citeshttps://doi.org/10.1021/ol2026747openalex-snapshot
Organocatalytic Asymmetric Neber Reaction for the Synthesis of 2H-Azirine Carboxylic Esters
inferred← citeshttps://doi.org/10.1021/ol400752sopenalex-snapshot
Acremolin from Acremonium strictum is N2,3-Etheno-2′-isopropyl-1-methylguanine, not a 1H-Azirine. Synthesis and Structural Revision
inferred← citeshttps://doi.org/10.1021/ol4030716openalex-snapshot
Formation of Functionalized 2H-Azirines through PhIO-Mediated Trifluoroethoxylation and Azirination of Enamines
inferred← citeshttps://doi.org/10.1021/ol802065dopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ol802890bopenalex-snapshot
Motualevic Acids A−F, Antimicrobial Acids from the Sponge Siliquariaspongia sp.
inferred← citeshttps://doi.org/10.1021/ol9006663openalex-snapshot
Simple Conversion of Enamines to 2 H -Azirines and Their Rearrangements under Thermal Conditions
inferred← citeshttps://doi.org/10.1039/a815607yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/a827013zopenalex-snapshot
Asymmetric synthesis of amino acids using sulfinimines (thiooxime S-oxides)
inferred← citeshttps://doi.org/10.1039/c1ob05324hopenalex-snapshot
Design and synthesis of pyrrolidine-containing sphingomimetics
inferred← citeshttps://doi.org/10.1039/c2np20055dopenalex-snapshot
Investigations of the marine flora and fauna of the Fiji Islands
inferred← citeshttps://doi.org/10.1039/c5ob02559aopenalex-snapshot
A Neber approach for the synthesis of spiro-fused 2H-azirine-pyrazolone
inferred← citeshttps://doi.org/10.1039/c6cc06388hopenalex-snapshot
Organocatalyzed nucleophilic addition of pyrazoles to 2H-azirines: asymmetric synthesis of 3,3-disubstituted aziridines and kinetic resolution of racemic 2H-azirines
inferred← citeshttps://doi.org/10.1039/c6cc07982bopenalex-snapshot
Direct catalytic enantioselective Mannich-type reaction of dichloroacetonitrile using bis(imidazoline)-Pd catalysts
inferred← citeshttps://doi.org/10.1039/c6ob02220kopenalex-snapshot
The organocatalytic asymmetric Neber reaction for the enantioselective synthesis of spirooxindole 2H-azirines
inferred← citeshttps://doi.org/10.1039/c7np00064bopenalex-snapshot
The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research
inferred← citeshttps://doi.org/10.1039/c9qo01177copenalex-snapshot
Cu-catalyzed C–N bond cleavage of 3-aminoindazoles for the C–H arylation of enamines
inferred← citeshttps://doi.org/10.1039/d0cc05379aopenalex-snapshot
Benzotetramisole catalyzed kinetic resolution of 2 H -azirines
inferred← citeshttps://doi.org/10.1039/d0qo00789gopenalex-snapshot
Kinetic resolution of 2 H -azirines via Cu( i )-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides
inferred← citeshttps://doi.org/10.1039/d4ob00410hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/np9931000029openalex-snapshot
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inferred← citeshttps://doi.org/10.1039/np9971400163openalex-snapshot
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inferred← citeshttps://doi.org/10.1055/s-0039-1691533openalex-snapshot
Asymmetric Neber Reaction in the Synthesis of Chiral 2-(Tetrazol-5-yl)-2H-Azirines
inferred← citeshttps://doi.org/10.1080/00304940209356770openalex-snapshot
PREPARATION, PROPERTIES AND SYNTHETIC APPLICATIONS OF 2H-AZIRINES A REVIEW
inferred← citeshttps://doi.org/10.1080/10286020.2013.844128openalex-snapshot
Two new compounds from an Indonesian sponge Dysidea sp.
inferred← citeshttps://doi.org/10.1080/10286020500172392openalex-snapshot
A new spiro-sesquiterpene from the sponge Dysidea fragilis
inferred← citeshttps://doi.org/10.1194/jlr.r800012-jlr200openalex-snapshot
Thematic Review Series: Sphingolipids. Biodiversity of sphingoid bases (“sphingosines”) and related amino alcohols
inferred← citeshttps://doi.org/10.3354/meps116125openalex-snapshot
Variation of 2,3.4-tribromopyrrole and its sodium sulfamate salt in the hemichordate Saccoglossus kowalevskii
inferred← citeshttps://doi.org/10.3390/md22070302openalex-snapshot
Streptomyces-Fungus Co-Culture Enhances the Production of Borrelidin and Analogs: A Genomic and Metabolomic Approach
inferred← citeshttps://doi.org/10.3390/molecules27051717openalex-snapshot
Anti-Inflammatory Dysidazirine Carboxylic Acid from the Marine Cyanobacterium Caldora sp. Collected from the Reefs of Fort Lauderdale, Florida
inferred← citeshttps://doi.org/10.3390/molecules28010275openalex-snapshot
5-Chloroisoxazoles: A Versatile Starting Material for the Preparation of Amides, Anhydrides, Esters, and Thioesters of 2H-Azirine-2-carboxylic Acids
inferred← citeshttps://doi.org/10.3762/bjoc.14.123openalex-snapshot
Synthesis of trifluoromethylated 2 H -azirines through Togni reagent-mediated trifluoromethylation followed by PhIO-mediated azirination
inferred← citeshttps://doi.org/10.3762/bjoc.20.264openalex-snapshot
Synthesis of 2 H -azirine-2,2-dicarboxylic acids and their derivatives
inferred← citeshttps://doi.org/10.5059/yukigoseikyokaishi.78.1126openalex-snapshot
Chemistry of 2H-Azirines from Old to New — Selective Synthesis and Transformation
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