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Evidence for oxirene intermediates in the peroxidation of acetylenes

https://doi.org/10.1021/ja00804a070
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inferred← citeshttps://doi.org/10.2139/ssrn.4809286openalex-extracted
Oxirene and Thiirene: Molecular Aggregation and Interaction with Water
inferred← citeshttps://doi.org/10.1002/9780470187203.ch1openalex-snapshot
Oxiranes
inferred← citeshttps://doi.org/10.1002/9780470771730.ch17openalex-snapshot
Polar reaction mechanisms involving peroxides in solution
inferred← citeshttps://doi.org/10.1002/chin.197404144openalex-snapshot
ChemInform Abstract: EVIDENCE FOR OXIRENE INTERMEDIATES IN THE PEROXIDATION OF ACETYLENES
inferred← citeshttps://doi.org/10.1002/jlac.197519750205openalex-snapshot
Synthese und Stabilität von 2,3‐Dichloroxiranen
inferred← citeshttps://doi.org/10.1002/jlac.197619761218openalex-snapshot
Organische Peroxide, XV. Oxirene als Zwischenstufen der basenkatalysierten Reaktion von elektronenarmen Alkinen mit Wasserstoffperoxid
inferred← citeshttps://doi.org/10.1002/kin.550070408openalex-snapshot
The role of solvent in some oxygen‐transfer reactions of peroxy compounds
inferred← citeshttps://doi.org/10.1007/978-1-4020-6973-4_3openalex-snapshot
Oxirene
inferred← citeshttps://doi.org/10.1007/978-1-4684-3728-7_10openalex-snapshot
Computer Chemistry Studies of Organic Reactions: The Wolff Rearrangement
inferred← citeshttps://doi.org/10.1007/s00894-024-06193-8openalex-snapshot
Constructing, in silico, molecular self-aggregates and micro-hydrated complexes of oxirene and thiirene
inferred← citeshttps://doi.org/10.1016/0040-4039(75)80012-8openalex-snapshot
Concerning the cycloelimination route to oxirenes
inferred← citeshttps://doi.org/10.1016/b978-0-12-470501-2.50009-7openalex-snapshot
Some Pericyclic Reactions of Carbenes
inferred← citeshttps://doi.org/10.1016/b978-0-12-697252-8.50008-xopenalex-snapshot
Oxidations with Peroxy Acids and other Peroxides
inferred← citeshttps://doi.org/10.1016/b978-0-444-41565-3.50021-1openalex-snapshot
10.1016/b978-0-444-41565-3.50021-1
inferred← citeshttps://doi.org/10.1016/b978-0-444-42030-5.50013-0openalex-snapshot
Additions to Acetylenes and Allenes
inferred← citeshttps://doi.org/10.1016/b978-008096519-2.00111-9openalex-snapshot
Oxiranes and Oxirenes
inferred← citeshttps://doi.org/10.1016/b978-008096519-2.00135-1openalex-snapshot
Volume 7 References
inferred← citeshttps://doi.org/10.1016/j.poly.2009.02.045openalex-snapshot
Electron spin density distribution of a series of nitroxide radicals with five-member ring as studied by solid-state 1H, 2H and 13C NMR
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)71475-4openalex-snapshot
Chemical evidence for oxirene intermediates
inferred← citeshttps://doi.org/10.1016/s0040-4039(01)83728-xopenalex-snapshot
Reinvestigation of the photodecomposition of 3-diazo-4-heptanone
inferred← citeshttps://doi.org/10.1021/ja001707oopenalex-snapshot
Alkyne Oxidations by cis-Dioxoruthenium(VI) Complexes. A Formal [3 + 2] Cycloaddition Reaction of Alkynes with cis-[(Cn*)(CF3CO2)RuVIO2]ClO4 (Cn* = 1,4,7-Trimethyl-1,4,7-triazacyclononane)
inferred← citeshttps://doi.org/10.1039/d3qo00236eopenalex-snapshot
Regio- and stereoselective oxidative conversion of alkynes to sulfenylated α,β-unsaturated carbonyls
inferred← citeshttps://doi.org/10.1246/bcsj.56.1133openalex-snapshot
Mechanism for the Oxidative Cleavage of Electron-deficient Acetylenes with Alkaline Hydrogen Peroxide
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