Combination of Transition Metals-(2,4-Pentanedionate) and P2O5 as a Regioselective Catalytic System for Nitric Acid Nitration of Ar-Himachalene

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ISSN Print: 2160-6951
ISSN Online: 2160-696X
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"Combination of Transition Metals-(2,4-Pentanedionate) and P2O5 as a Regioselective Catalytic System for Nitric Acid Nitration of Ar-Himachalene"
written by Issam Hossini, Mohamed Anoir Harrad, Brahim Boualy, Mustapha Ait Ali, Larbi El Firdoussi, Abdallah Karim,
published by Green and Sustainable Chemistry, Vol.1 No.3, 2011

has been cited by the following article(s):

[1]	Theoretical investigation of the mechanism and regioselectivity of the 3-isopropyl-1, 6-dimethyl-naphthalene and ar-himachalene in nitration reaction: a MEDT study
	Theoretical Chemistry Accounts, 2022

[2]	Synthesis and Characterization of New Chalcone Derivatives of Aryl-Himachalene
	2020

[3]	Synthetic studies towards sesquiterpene butenolides,(S)-ar-himachlene, development of synthetic methodology and it's application in synthesis of (R) …
	2016

[4]	Aerobic oxidation of aryl-himachalene using a combination of N-hydroxy phthalimide and cobalt (II) acetoacetate
	Chemistry and Materials Research, 2014

[5]	Enantioselective synthesis of the essential oil and pheromonal component ar-himachalene by a chiral pool and chirality induction approach
	Tetrahedron: Asymmetry, 2012

[6]	Enantioselective synthesis of the essential oil and pheromonal component< i> ar-himachalene by a chiral pool and chirality i
	Tetrahedron: Asymmetry, Elsevier, 2012

[1]	Theoretical investigation of the mechanism and regioselectivity of the 3-isopropyl-1,6-dimethyl-naphthalene and ar-himachalene in nitration reaction: a MEDT study Theoretical Chemistry Accounts, 2022 DOI:10.1007/s00214-022-02869-7

[2]	Synthesis and Characterization of New Chalcone Derivatives of Aryl-Himachalene Organic Preparations and Procedures International, 2020 DOI:10.1080/00304948.2020.1751562

[3]	Enantioselective synthesis of the essential oil and pheromonal component ar-himachalene by a chiral pool and chirality induction approach Tetrahedron: Asymmetry, 2012 DOI:10.1016/j.tetasy.2012.09.008

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