Magnetic hydroxyapatite-immobilized 1,4-diazabicyclo [2.2.2] octane as a highly efficient and eco-friendly nanocatalyst for the promotion of nucleophilic substitution reactions of benzyl halides under green conditions

Substitution Reactions ◽

Highly Efficient ◽

Benzyl Halides ◽

Green Conditions

β-Cyclodextrin based polyurethane as eco-friendly polymeric phase transfer catalyst in nucleophilic substitution reactions of benzyl halides in water: An efficient route to synthesis of benzyl thiocyanates and acetates

Catalysis Science & Technology ◽

10.1039/c2cy00375a ◽

2012 ◽

Vol 2 (5) ◽

pp. 1056 ◽

Cited By ~ 17

Author(s):

Ali Reza Kiasat ◽

Simin Nazari

Keyword(s):

Phase Transfer ◽

Phase Transfer Catalyst ◽

Substitution Reactions ◽

Benzyl Halides ◽

Efficient Route

Magnetic nanoparticles grafted with β-cyclodextrin–polyurethane polymer as a novel nanomagnetic polymer brush catalyst for nucleophilic substitution reactions of benzyl halides in water

Journal of Molecular Catalysis A Chemical ◽

10.1016/j.molcata.2012.08.012 ◽

2012 ◽

Vol 365 ◽

pp. 80-86 ◽

Cited By ~ 68

Author(s):

Ali Reza Kiasat ◽

Simin Nazari

Keyword(s):

Magnetic Nanoparticles ◽

Polymer Brush ◽

Substitution Reactions ◽

Preparation of novel magnetic dicationic ionic liquid polymeric phase transfer catalyst and their application in nucleophilic substitution reactions of benzyl halides in water

Journal of Molecular Liquids ◽

10.1016/j.molliq.2014.12.009 ◽

2015 ◽

Vol 202 ◽

pp. 34-39 ◽

Cited By ~ 19

Author(s):

Bijan Mombani Godajdar ◽

Bita Ansari

Keyword(s):

Ionic Liquid ◽

Phase Transfer ◽

Phase Transfer Catalyst ◽

Substitution Reactions ◽

Benzyl Halides ◽

Dicationic Ionic Liquid

Highly Efficient Chain End Derivatization of Selenol-Ended Polystyrenes by Nucleophilic Substitution Reactions

Macromolecular Chemistry and Physics ◽

10.1002/macp.201600485 ◽

2016 ◽

Vol 218 (4) ◽

pp. 1600485 ◽

Cited By ~ 9

Author(s):

Weihong Lu ◽

Xiaowei An ◽

Feng Gao ◽

Jian Zhu ◽

Nianchen Zhou ◽

...

Keyword(s):

Substitution Reactions ◽

Highly Efficient

957. Nucleophilic substitution reactions of benzyl halides. Part I. The reaction of benzyl chloride with partly aqueous solvents

Journal of the Chemical Society (Resumed) ◽

10.1039/jr9570004747 ◽

1957 ◽

pp. 4747 ◽

Cited By ~ 2

Author(s):

B. Bensley ◽

G. Kohnstam

Keyword(s):

Benzyl Chloride ◽

Substitution Reactions ◽

Oligoethylene Glycols as Highly Efficient Mutifunctional Promoters for Nucleophilic-Substitution Reactions

Chemistry - A European Journal ◽

10.1002/chem.201102455 ◽

2012 ◽

Vol 18 (13) ◽

pp. 3918-3924 ◽

Cited By ~ 27

Author(s):

Vinod H. Jadhav ◽

Seung Ho Jang ◽

Hwan-Jeong Jeong ◽

Seok Tae Lim ◽

Myung-Hee Sohn ◽

...

Keyword(s):

Substitution Reactions ◽

Highly Efficient ◽

Oligoethylene Glycols

PEG‐DIL‐based MnCl42−: A novel phase transfer catalyst for nucleophilic substitution reactions of benzyl halides

Applied Organometallic Chemistry ◽

10.1002/aoc.4647 ◽

2018 ◽

pp. e4647

Author(s):

Bijan Mombeni Goodajdar ◽

Farideh Akbari ◽

Jamal Davarpanah

Keyword(s):

Phase Transfer ◽

Phase Transfer Catalyst ◽

Substitution Reactions ◽

994. Nucleophilic substitution reactions of benzyl halides. Part II. Rates and product proportions for the solvolysis of benzyl chloride in ethanol–water mixtures

Journal of the Chemical Society (Resumed) ◽

10.1039/jr9570004970 ◽

1957 ◽

Vol 0 (0) ◽

pp. 4970-4973 ◽

Cited By ~ 2

Author(s):

G. Kohnstam ◽

P. R. Robinson

Keyword(s):

Benzyl Chloride ◽

Substitution Reactions ◽

Synthesis of Diastereomeric Pyrrolidine Sulfamides via Anchimerically Assisted Nucleophilic Substitution Reactions

Letters in Organic Chemistry ◽

10.2174/1570178615666180110162202 ◽

2018 ◽

Vol 15 (5) ◽

pp. 352-358

Author(s):

Jorge Vargas-Caporali ◽

Arie van der Lee ◽

Georges Dewynter ◽

Eusebio Juaristi

Keyword(s):

Nucleophilic Substitution Reactions

Substitution Reactions ◽

The unexpected reactivity of 9-iodo-nido-carborane: from nucleophilic substitution reactions to the synthesis of tricobalt tris(dicarbollide) Na[4,4′,4′′-(MeOCH2CH2O)3-3,3′,3′′-Co3(μ3-O)(μ3-S)(1,2-C2B9H10)3]

Dalton Transactions ◽

10.1039/d0dt03857a ◽

2021 ◽

Vol 50 (7) ◽

pp. 2671-2688

Author(s):

Marina Yu. Stogniy ◽

Sergey A. Anufriev ◽

Akim V. Shmal'ko ◽

Sergey M. Antropov ◽

Aleksei A. Anisimov ◽

...

Keyword(s):

Nucleophilic Substitution Reactions

Substitution Reactions ◽

An unusual reactivity of 9-iodo-nido-carborane [9-I-7,8-C2B9H11]− towards nucleophiles under strong basic conditions was revealed.