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Synthetic approaches toward the bi(2H-azirine) system

https://doi.org/10.1021/jo01333a001
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inferred← citeshttps://doi.org/10.2139/ssrn.4675520openalex-extracted
inferred← citeshttps://doi.org/10.1002/0471264180.or034.01openalex-snapshot
Reductions by Metal Alkoxyaluminum Hydrides
inferred← citeshttps://doi.org/10.1002/0471264180.or036.03openalex-snapshot
Reductions by Metal Alkoxyaluminum Hydrides. Part II . Carboxylic Acids and Derivatives, Nitrogen Compounds, and Sulfur Compounds
inferred← citeshttps://doi.org/10.1002/1521-3757(20010105)113:1<173::aid-ange173>3.0.co;2-vopenalex-snapshot
Synthese von 1,4-Diazidobuta-1,3-dienen durch elektrocyclische Ringöffnung: Vorstufen für Bi-2H-azirin-2-yle und deren Valenzisomerisierung zu Diazabenzolen
inferred← citeshttps://doi.org/10.1002/1521-3773(20010105)40:1<174::aid-anie174>3.0.co;2-8openalex-snapshot
Synthesis of 1,4-Diazidobuta-1,3-dienes by Electrocyclic Ring Opening: Precursors for Bi-2H-azirin-2-yls and Their Valence Isomerization to Diazabenzenes Reactions of Unsaturated Azides, Part 13. This work was supported by the Fonds der Chemische Industrie. We thank Dr. M. Hagedorn, Dr. J.…
inferred← citeshttps://doi.org/10.1002/9780470682517.ch5openalex-snapshot
The Chemistry of Vinyl, Allenyl, and Ethynyl Azides
inferred← citeshttps://doi.org/10.1002/9783527619573.ch7openalex-snapshot
Acceptor‐Substituted Allenes
inferred← citeshttps://doi.org/10.1002/ange.19901020126openalex-snapshot
2‐Methylen‐2H‐azirine durch Photolyse von 1‐Azidoallenen
inferred← citeshttps://doi.org/10.1002/anie.199001031openalex-snapshot
2‐Methylene‐2H‐azirines by Photolysis of 1‐Azidoallenes
inferred← citeshttps://doi.org/10.1002/chem.200600318openalex-snapshot
Experimental and Theoretical Characterization of the Valence Isomerization of Bi‐2H‐azirin‐2‐yls to Diazabenzenes
inferred← citeshttps://doi.org/10.1002/chem.201101220openalex-snapshot
Experimental and Theoretical Characterization of the Aromatization, Epimerization, and Fragmentation Reactions of Bi‐2H‐azirin‐2‐yls Prepared from 1,4‐Diazidobuta‐1,3‐dienes
inferred← citeshttps://doi.org/10.1002/chin.198003250openalex-snapshot
ChemInform Abstract: SYNTHETIC APPROACHES TOWARD THE BI(2H‐AZIRINE) SYSTEM
inferred← citeshttps://doi.org/10.1002/jhet.4415openalex-snapshot
Synthesis of various functionalized 2H‐azirines: An updated library
inferred← citeshttps://doi.org/10.1002/jhet.5570450203openalex-snapshot
Synthesis of azirines containing aldehyde functionality and their utilization as synthetic tools for five membered oxazoles and isoxazoles
inferred← citeshttps://doi.org/10.1002/prac.19983400802openalex-snapshot
Ring Transformations in Tetrazole Chemistry
inferred← citeshttps://doi.org/10.1007/978-3-642-69037-2_11openalex-snapshot
References
inferred← citeshttps://doi.org/10.1007/bf00503523openalex-snapshot
Advances in the chemistry of tetrazoles (review)
inferred← citeshttps://doi.org/10.1016/0040-4039(94)85209-xopenalex-snapshot
Attempted generation and structure of the 4-(1,2,4-triazoyl) cation
inferred← citeshttps://doi.org/10.1016/b0-08-044655-8/00069-6openalex-snapshot
Functions Incorporating a Halogen and Another Heteroatom Group Other Than a Chalcogen
inferred← citeshttps://doi.org/10.1016/b978-0-08-052349-1.00171-2openalex-snapshot
Functional Group Transformations via Carbonyl Derivatives
inferred← citeshttps://doi.org/10.1016/j.forc.2024.100558openalex-snapshot
Forensic implications of novel synthesis of cathinone derivatives by Neber and modified Neber rearrangements
inferred← citeshttps://doi.org/10.1016/j.tet.2013.02.020openalex-snapshot
Recent advances in 2H-azirine chemistry
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.07.190openalex-snapshot
Alkoxyl radical fragmentation of 3-azido-2,3-dideoxy-2-halo-hexopyranoses: a new entry to chiral polyhydroxylated 2-azido-1-halo-1-alkenes
inferred← citeshttps://doi.org/10.1016/s0022-328x(00)83951-0openalex-snapshot
Lithium
inferred← citeshttps://doi.org/10.1016/s0040-4020(01)00598-1openalex-snapshot
Synthesis of 2-halo-2H-azirines
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)74549-7openalex-snapshot
On the stability of azirinyl and diazirinyl cations
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)87336-0openalex-snapshot
Azirinyl and diazirinyl (chloride) ion pairs as intermediates
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)81783-4openalex-snapshot
Chloroazirines-conversion to azacyclopropenium cations azidoazirines and biazirines
inferred← citeshttps://doi.org/10.1016/s0040-4039(98)02413-7openalex-snapshot
Synthesis of 2-halo-2H-azirines from phosphorus ylides
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00222openalex-snapshot
Oxidation of Tetraphenylhexaazaanthracene: Accessing a Scissor Dimer of a 16π Biscyanine
inferred← citeshttps://doi.org/10.1021/jo800182yopenalex-snapshot
Synthesis of Polyhydroxylated 2H-Azirines and 2-Halo-2H-azirines from 3-Azido-2,3-dideoxyhexopyranoses by Alkoxyl Radical Fragmentation
inferred← citeshttps://doi.org/10.2116/analscix.22.x25openalex-snapshot
Crystal Structure of Z-2-Amino-1-phenyl-3-phenylsulfonylprop-2-en-1-one
inferred← citeshttps://doi.org/10.2139/ssrn.4089606openalex-snapshot
1,4,2-Diazaborole-Type Heterocycle from 2h-Azirine-2-Carboxylate and [(Alkylamino)Methyl]Trifluoroborate
inferred← citeshttps://doi.org/10.3390/molecules201219848openalex-snapshot
Synthesis of New 2-Halo-2-(1H-tetrazol-5-yl)-2H-azirines via a Non-Classical Wittig Reaction
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