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Mendeleev Communications, 2006, Volume 16, Issue 2, Pages 98–100
DOI: https://doi.org/10.1070/MC2006v016n02ABEH002219
(Mi mendc3537)
 

This article is cited in 10 scientific papers (total in 10 papers)

The reaction of hex-1-yne with 2,2,2-trichlorobenzo[d]-1,3,2-dioxaphosphole

E. N. Varaksina, V. F. Mironov, R. Z. Musin, A. I. Konovalov

A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
Abstract: The title reaction gives 2,6-dichloro- and 2,8-dichloro-2-oxo-4-butylbenzo[e]-1,2-oxaphosphorinines in a ratio of 9:1.
Document Type: Article
Language: English


Citation: E. N. Varaksina, V. F. Mironov, R. Z. Musin, A. I. Konovalov, “The reaction of hex-1-yne with 2,2,2-trichlorobenzo[d]-1,3,2-dioxaphosphole”, Mendeleev Commun., 16:2 (2006), 98–100
Linking options:
  • https://www.mathnet.ru/eng/mendc3537
  • https://www.mathnet.ru/eng/mendc/v16/i2/p98
  • This publication is cited in the following 10 articles:
    1. D. A. Tatarinov, E. A. Mikulenkova, N. V. Terekhova, A. V. Nemtarev, A. P. Lyubina, A. D. Voloshina, A. S. Sapunova, A. B. Dobrynin, I. A. Litvinov, V. F. Mironov, “Synthesis and antimicrobial activity of alkyl[2-(5-chloro-2-hydroxyphenyl)hex-1-en-1-yl]diphenylphosphonium salts”, Russ Chem Bull, 73:12 (2024), 3699  crossref
    2. A. V. Nemtarev, I. O. Nasibullin, R. R. Fayzullin, L. R. Grigor'eva, V. F. Mironov, “2,2,2-Trichloro-4-methoxy-1,3,2-benzodioxaphosphole in the reactions with terminal acetylenes”, Mendeleev Commun., 30:1 (2020), 34–37  mathnet  crossref
    3. Cheol‐Eui Kim, Taekyu Ryu, Sanghyuck Kim, Kooyeon Lee, Chang‐Hee Lee, Phil Ho Lee, “Gold‐Catalyzed Hydroarylation of Aryl Alkynylphosphonates for the Synthesis of Phosphacoumarins”, Adv Synth Catal, 355:14-15 (2013), 2873  crossref
    4. A. S. Aniskin, A. V. Nemtarev, V. F. Mironov, “Reaction of 2′,2′,2′,2″,2″,2″-Hexabromo-1,4-di(benzo-1,3,2-dioxaphosphol-5-yl)benzene with phenylacetyleneom”, Russ J Org Chem, 49:5 (2013), 768  crossref
    5. V. F. Mironov, A. V. Nemtarev, “Reaction of P,P,P-trihalogenbenzo-1,3,2-dioxaphospholes with terminal acetylenes: Phosphorus-carbon bond formation and the ipso-substitution of oxygen by carbon”, Ref. J. Chem., 1:1 (2011), 27  crossref
    6. I. S. Ryzhkina, L. I. Murtazina, A. V. Nemtarev, V. F. Mironov, A. I. Konovalov, “Supramolecular water systems based on the new amphiphilic phosphacoumarins: synthesis, self-organizations and reactivity”, Mendeleev Commun., 20:3 (2010), 148–150  mathnet  crossref
    7. A. V. Nemtarev, E. N. Varaksina, V. F. Mironov, R. Z. Musin, A. I. Konovalov, “Predominant formation of 4-butyl-2,5-dichloro-2-oxo-1,2λ5-benzoxaphosphinine-6-carbonyl chloride in the reaction of 2,2,2-trichloro-1,3,2λ5-benzodioxaphosphole-5-carbonyl chloride with hex-1-yne”, Russ J Org Chem, 43:3 (2007), 468  crossref
    8. A. V. Nemtarev, E. N. Varaksina, V. F. Mironov, R. Z. Musin, A. I. Konovalov, “Regioselectivity of the reaction of 4,6-di-tert-butyl-2,2,2-trichloro-1,3,2λ5-benzodioxaphosphole with hex-1-yne. ipso substitution of tert-butyl group”, Russ J Org Chem, 43:11 (2007), 1737  crossref
    9. A. V. Nemtarev, V. F. Mironov, E. N. Varaksina, Yu. V. Nelyubina, M. Yu. Antipin, R. Z. Musin, A. I. Konovalov, “Pyridine and benzyltriethylammonium chloride ate-complexes of 2,2,2-trichlorobenzo[d]-1,3,2-dioxaphosphole in reactions with alk-1-ynes”, Mendeleev Commun., 17:6 (2007), 327–329  mathnet  crossref
    10. Andrey V. Nemtarev, Elena N. Varaksina, Vladimir F. Mironov, Rashid Z. Musin, Alexander I. Konovalov, “The Reaction of Hex‐1‐yne with 2,2,2‐Trichlorobenzo[d]‐1,3,2‐dioxaphosphole.”, ChemInform, 37:37 (2006)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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