Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ashutosh V. Joshi"'
Autor:
Gaik-Khuan Chuah, Stephan Jaenicke, Ashutosh V. Joshi, Yoel Sasson, Sudip Mukhopadhyay, Nida Qafisheh
Publikováno v:
Industrial & Engineering Chemistry Research. 46:3016-3023
Potassium phosphate is reported as a remarkably active and selective solid base in phase-transfer-catalyzed alkylation reactions of alkaline-sensitive substrates such as esters and halides. The performance of potassium phosphate exceeded that of comm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba91a276007b81a2313056cfb2a9f1cb
https://doi.org/10.1021/ie060899e
https://doi.org/10.1021/ie060899e
Publikováno v:
Synthetic Communications. 35:2715-2722
High‐yield reductive homocoupling of benzotrichloride and benzal chloride followed by consecutive reductive dechlorination to 1,2‐dichlorostilbene and stilbene is effected in the presence of sodium formate as the reducing agent and Pd/C catalysts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f64bd83dfde0d802baf5d8504dbadb60
https://doi.org/10.1080/00397910500214458
https://doi.org/10.1080/00397910500214458
Publikováno v:
Synthetic Communications. 34:643-650
Aromatic and aliphatic aldehydes are selectively reduced to primary alcohols under mild conditions with potassium formate in the presence of Pd/C catalyst. The high selectivity obtained is attributed due to the presence of the basic potassium bicarbo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57d5f1d71223e1d6e1dbada35a6259c1
https://doi.org/10.1081/scc-120027711
https://doi.org/10.1081/scc-120027711
Publikováno v:
Advanced Synthesis & Catalysis, 344, 348-354. Wiley-VCH Verlag
The Heck reaction of chlorobenzene and substituted chlorobenzenes with styrene is performed in water using catalytic palladium on carbon. The presence of a reducing agent, a mild base, and a phase-transfer catalyst enhances the reactivity of chloroar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c08e46adef38108da5b13c4eec8ab85
https://doi.org/10.1002/1615-4169(200206)344:3/4<348::AID-ADSC348>3.0.CO
https://doi.org/10.1002/1615-4169(200206)344:3/4<348::AID-ADSC348>3.0.CO
Publikováno v:
Tetrahedron Letters. 46:3583-3585
Thiols are oxidized to the corresponding disulfides with a mild base, anhydrous potassium phosphate, under ambient conditions in the presence of air.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94dee625ce36055a683f70f972937279
https://doi.org/10.1016/j.tetlet.2005.03.040
https://doi.org/10.1016/j.tetlet.2005.03.040
Publikováno v:
Organic Process Research & Development. 8:568-570
Oxidative bromination of activated aromatic compounds using alkali metal bromide salts and aqueous nitric acid to the corresponding bromo-derivatives is achieved in a liquid−liquid, two-phase system under ambient conditions. Nitric acid offers a du
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc324d5885bf3a8b0f954140d87b5043
https://doi.org/10.1021/op030055w
https://doi.org/10.1021/op030055w
Publikováno v:
Organic Process Research & Development. 7:44-46
Reductive coupling of haloaryls and substituted haloaryls to the respective biaryls is effected in water with good selectivity, using a reducing agent such as formate salts and a base, NaOH, in the presence of a catalytic amount of PEG-400 and 5% Rh/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::061a491a1956c4b3e3e17110b54e2146
https://doi.org/10.1021/op020080m
https://doi.org/10.1021/op020080m
Publikováno v:
Organic Process Research & Development. 7:95-97
Highly selective nitration of phenol and substituted phenols to the corresponding nitro compounds is accomplished under mild conditions in a liquid−liquid two-phase system with dilute nitric acid (...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a48527c598234f6cb13deb92fcb80cf
https://doi.org/10.1021/op0200120
https://doi.org/10.1021/op0200120
Publikováno v:
ChemInform. 37
High‐yield reductive homocoupling of benzotrichloride and benzal chloride followed by consecutive reductive dechlorination to 1,2‐dichlorostilbene and stilbene is effected in the presence of sodium formate as the reducing agent and Pd/C catalysts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df498a91ebc614b6e90b1a47db02f671
https://doi.org/10.1002/chin.200609095
https://doi.org/10.1002/chin.200609095
Publikováno v:
ChemInform. 35
Effective chlorination of 2,3,5,6-tetrachloropyridine to pentachloropyridine was realized under mild phase transfer conditions with carbon tetrachloride and 50% NaOH or solid K 3 PO 4 . Mechanistic study of this reaction indicated the possibility of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ae9dcb3d3537f3152d10f69b9f6deb3
https://doi.org/10.1002/chin.200440141
https://doi.org/10.1002/chin.200440141