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Reagents supported

P. Pfeifer, in Preparative Chemistry Using Supported Reagents, P. Laszlo, ed.. Academic, New York, 1987. [Pg.594]

One widely used method of formation of protected compounds involves polymer-supported reagents, with the advantage of simple workup by filtration and automated syntheses, especially of polypeptides. Polymer-supported reagents are used to protect a terminal — COOH group as a polymer-bound ester (RCOOR —( ) during peptide syntheses, to protect primary alcohols as... [Pg.3]

R. J. Booth and J.C. Hodges, Solid-supported reagent strategies for rapid purification of combinatorial synthesis products, Acc Chem Res 32 18-26 1999. [Pg.78]

S. V. Ley, l.R. Baxendale, G. Brusotti, M. Caldarelli, A. Massi and M. Nesi, Solid-supported Reagents for Multi-step Organic Synthesis Preparation and Application, II Farmaco 57 321-330 2002. [Pg.78]

S. Bhattacharyya, Polymer-supported reagents and catalysts Recent advances in synthetic applications. Comb Chem High Throughput Screening 3 65-92 2000. [Pg.79]

Organic dyes which are not complexed or are salts of metals are included in Chapter 4 (use the CAS Registry Numbers to find them). Commercially available polymer supported reagents are indicated with under the appropriate reagent. [Pg.389]

Tetra-n-propylammonium perruthenate (TPAP, tetrapropyl tetraoxoruthenate) [114615-82-6] M 351.4, m 160"(dec). It is a strong oxidant and may explode on heating. It can be washed with aq n-propanol, then H2O and dried over KOH in a vac. It is stable at room temp but best stored in a refrigerator. It is sol in CH2CI2 and MeCN. [Dengel et al. Transition Met Chem 10 98 1985 Griffith et al. J Chem Soc, Chem Commun 1625 1987.] Polymer supported reagent is available commercially. [Pg.483]

Polymer supported reagents, catalysts, protecting groups, and mediators can be used in place of the corresponding small molecule materials (Sherrington, 1991 Sundell and Nasman, 1993). The reactive species is tightly bound to a macromolecular support which immobilizes it. This generally makes toxic, noxious, or corrosive materials much safer. The use of polystyrene sulfonic acid catalyst for the manufacture of methyl r-butyl... [Pg.37]

Gupta et al. reported that the Vilsmeier-Haack cyclisation of acetanilides 20 using supported reagents and microwave-irradiation in solvent-free conditions is rapid and efficient. Reaction yields are good, although only a few activated derivatives have been investigated. [Pg.447]

It years, there has been a considerable growth of interest in the catalysis of organic IS by inorganic reagents supported on high surface areas, Envirocat, a new family of supported reagents, which exhibits both Bronstead and Lev/is acid character, are ideal for environmentally friendly chemistry. These reagents are non-toxic powders that can be easily... [Pg.40]

Viewed in conjunction with the solid-like, nonvolatile nature of ionic liquids, it is apparent that TSILs can be thought of as liquid versions of solid-supported reagents. Unlike solid-supported reagents, however, TSILs possess the added advantages of kinetic mobility of the grafted functionality and an enormous operational surface area (Figure 2.3-1). It is this combination of features that makes TSILs an aspect of ionic liquids chemistry that is poised for explosive growth. [Pg.34]

Figure 2.3-1 Substrate interactions with (I to r) solid-supported reagent, polymer gel support-... Figure 2.3-1 Substrate interactions with (I to r) solid-supported reagent, polymer gel support-...
Amos prepared his polymer-supported reagent in two steps from commercially available polystyrene beads (bromination, then condensation with lithium diphenylphosphide). He found that a useful range of sulphoxides could be reduced effectively, in good yields and in a few hours, to give clean samples of sulphides. [Pg.928]

Two polymer-supported reagents have been developed for the oxidation of sulphoxides to sulphones these involve peracid groups150, and bound hypervalent metals activated by t-butyl hydroperoxide151,152. [Pg.985]

Polychloromethylsulphonylbiphenyls, mass spectra of 154, 155 Polyenes, synthesis of 771 Polymerization, of sulphoxides 846 Polymer-supported reagents 928 Polymorphonuclear leukocytes 854 Poly(olefin sulphonejs, radiolysis of 916-922 Polysulphones, radiolysis of 913 Population analysis 14, 15, 21, 22 Propargylic sulphenates, rearrangement of 736-739... [Pg.1203]

A solid-phase Diels-Alder reaction that uses polymer-supported reagents has recently attracted considerable attention and its use is expanding rapidly. [Pg.149]

Fig. 29 Microwave-promoted multicomponent synthesis of polysubstituted thiophenes on soluble PEG support. Reagents and conditions a NCCH2OOH, DCC, DMAP, CHCI3, MW 130 W, 5 min b RCOCH2R, S8, diisopropylethylamine, MW 130 W, 15 min c R"COCl, di-isopropylethylamine, 0 °C to rt, 3 h d 1% KCN in CH3OH, o.n. R = H or alkyl R = alkyl or acyl R" = CH3, Ph... Fig. 29 Microwave-promoted multicomponent synthesis of polysubstituted thiophenes on soluble PEG support. Reagents and conditions a NCCH2OOH, DCC, DMAP, CHCI3, MW 130 W, 5 min b RCOCH2R, S8, diisopropylethylamine, MW 130 W, 15 min c R"COCl, di-isopropylethylamine, 0 °C to rt, 3 h d 1% KCN in CH3OH, o.n. R = H or alkyl R = alkyl or acyl R" = CH3, Ph...
Fig. 34 Preparation of a 4-thiazolidinone library using an ionic liquid support. Reagents and conditions a MW 100 °C, l-2h, open vessel b R"NH2, t-BuOK, MW 100-150°C, 10-20 min. R = H, Me, CH2COOH R = Pr, i-Pr, i-Bu, Bn, piperonyl, CH2CH(OMe)2, CH2CH CH2 R" = Pr, Bu, Bn, or cyclic derivatives as piperonyl, piperidine, pyrrolidine,... Fig. 34 Preparation of a 4-thiazolidinone library using an ionic liquid support. Reagents and conditions a MW 100 °C, l-2h, open vessel b R"NH2, t-BuOK, MW 100-150°C, 10-20 min. R = H, Me, CH2COOH R = Pr, i-Pr, i-Bu, Bn, piperonyl, CH2CH(OMe)2, CH2CH CH2 R" = Pr, Bu, Bn, or cyclic derivatives as piperonyl, piperidine, pyrrolidine,...
Fig. 35 Preparation of 2-thioxo tetrahydropyrimidin-4-(2H)-ones on ionic hquid support. Reagents and conditions a R N = C = S, MeCN, rt, 18 h b Et2NH, MW, 120 °C, 15-45 min. R = Pr, i-PrCH2, PhCH2 R = Me, Bu... Fig. 35 Preparation of 2-thioxo tetrahydropyrimidin-4-(2H)-ones on ionic hquid support. Reagents and conditions a R N = C = S, MeCN, rt, 18 h b Et2NH, MW, 120 °C, 15-45 min. R = Pr, i-PrCH2, PhCH2 R = Me, Bu...
Fig. 36 Synthesis of a polysubstituted pyran on ionic liquid support. Reagents and conditions a ethyl acetoacetate, MW 200 W, reflux, 10 min b arylidenemalononitriles, pyridine, MeCN, MW 200 W, reflux, 15-20 min c NaOMe, MeOH, rt, 6h... Fig. 36 Synthesis of a polysubstituted pyran on ionic liquid support. Reagents and conditions a ethyl acetoacetate, MW 200 W, reflux, 10 min b arylidenemalononitriles, pyridine, MeCN, MW 200 W, reflux, 15-20 min c NaOMe, MeOH, rt, 6h...
Synthesis of Heterocycles Using Polymer-Supported Reagents under Microwave Irradiation... [Pg.129]

Synthesis of Heteroq cles Using Polymer-Supported Reagents... [Pg.131]


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Applications of Supported Reagents

Base reagents, solid supported

Cerium reagents silica support

Charcoal-supported reagents

Chemical libraries, polymer-supported reagents

Chromium reagents silica support

Chromium reagents solid-supported

Clay-supported reagents

Electrophilic reagents, solid supported

Esterifications using supported reagents

Heterocycles polymer-supported reagents

Horner-Emmons Reagents on Supports

Iodine reagents ionic-liquid-supported

Iodine reagents polymer-supported

Ionic liquid-supported synthesis reagents

Ionic-Liquid-Supported Recyclable Hypervalent Iodine(III) Reagents

Ionic-liquid-supported reagents

Leaching, from supported metal reagents

Microwave inorganic supported reagent

Microwave reactions with polymer-supported reagents

Multi-supported reagents

Multistep Use of Supported Reagents in Natural Product Synthesis

Nucleophilic reagents, solid supporte

Oligonucleotides polymer-supported reagents

Organic Synthesis Using Microwaves and Supported Reagents

Osmium reagents, supported

Other Supported Coupling Reagents

Oxidation solid-supported reagents

Oxidation using supported reagents

Oxidation with Multi Supported Reagents

Polymer supported reagents acidic

Polymer supported reagents in synthesis

Polymer supported reagents industrial applications

Polymer supported reagents preparation

Polymer supported reagents reuse

Polymer supports for reagents, catalysts, and drug release

Polymer-Supported Iodine(III) Reagents

Polymer-Supported Reagents Preparation and Use in Parallel Organic Synthesis

Polymer-Supported Reducing Reagents

Polymer-supported Burgess reagent

Polymer-supported Mukaiyama reagent

Polymer-supported Reagents and Scavengers

Polymer-supported Wittig reagent

Polymer-supported catalysts and reagents

Polymer-supported hypervalent iodine reagent

Polymer-supported quenching reagents

Polymer-supported reagents

Polymer-supported reagents 1,3,4-oxadiazole synthesis

Polymer-supported reagents Wittig reactions

Polymer-supported reagents acylation

Polymer-supported reagents alkene hydrogenation

Polymer-supported reagents alkylation

Polymer-supported reagents carboxylic acid synthesis

Polymer-supported reagents coupling

Polymer-supported reagents ester synthesis

Polymer-supported reagents groups

Polymer-supported reagents multistep synthesis applications

Polymer-supported reagents overview

Polymer-supported reagents reactions reviewed

Polymer-supported reagents reductive aminations

Polymer-supported reagents scavengers

Polymer-supported reagents scavenging

Polymer-supported reagents solvent considerations

Polymer-supported reagents sulfonic acid

Polymer-supported reagents synthesis

Polymer-supported reagents transition metal catalysts

Polymer-supported reagents, functional

Polymer-supported reagents, functional groups distribution

Polymer-supported reagents, general application

Polymer-supported thionating reagent

Polymer-supported, acid reagents

Polystyrene supported reagents

Preparation of Supported Reagents

Radical Reactions Using Supported Reagents

Reaction polymer-supported reagent

Reagents polymer-supported, degree

Reagents supported, advantages

Reductions using polymer supported reagents

Screening solid-supported reagent

Silica gel-supported reagents

Silica-supported reagents

Simultaneous multistep synthesis using several polymer-supported reagents

Solid support reagents

Solid-Supported Hypervalent Iodine Reagents

Solid-Supported Organotin Reagents

Solid-Supported Reagents and Scavengers

Solid-phase-supported reagents and scavengers

Solid-supported Reagents and Catalysts

Solid-supported reagents

Solid-supported reagents acylation

Solid-supported reagents alumina

Solid-supported reagents silica

Soluble Polymer-supported Reagents

Studying Supported Reagents

Sulfonation in synthesis of polymer supported reagent

Support reagent

Supported Reagent Chemistry

Supported Reagents and Scavengers in Multi-Step Organic Synthesis

Supported cerium reagents

Supported reagents activities

Supported reagents applications

Supported reagents composition

Supported reagents industrial applications

Supported reagents inorganic based

Supported reagents macroporous

Supported reagents polymer based

Supported reagents porosity

Supported reagents preparation

Supported reagents reuse

Supported reagents stability

Supported reagents surfaces

Supported reagents types

Synthesis of 1,3,4-oxadiazoles using polymer-supported Burgess reagent

Synthesis reagents, solid supported

Thallium reagents solid-supported

The use of solid supports and supported reagents in liquid phase organic reactions

The use of solid-supported reagents in noncatalytic flow processes

Three-Component Reactions Using Supported Reagents

Toluenesulfonyl Chloride and Related Reagents, Polymer-supported

Triphenylphosphine supported reagents

Types of Supported Reagents

Use of supported reagents

Wittig reagents polymer-bound, supports

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