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Synthesis allylic

Furo[3,4-d]pyridazine-1,4-diones synthesis, 4, 985 Furopyridazines, 4, 984 Furo[2,3-6]pyridine, 3-amino-synthesis, 4, 977 Furo[2,3-6]pyridine, 4-methyl-synthesis, 4, 976 Furo[2,3-6]pyridine, 6-methyl-synthesis, 4, 976 Furo[2,3-6]pyridine, 5-nitro-synthesis, 4, 977 Furo[3,2-c]pyridine, 4-allyl-synthesis, 4, 982 Furopyri dines H NMR, 4, 983 physical data, 4, 983 properties, 4, 982 synthesis, 4, 974-982 UV spectroscopy, 4, 983 Furo[6]pyri dines HMO data, 4, 975 Furo[2,3-6]pyri dines synthesis, 4, 974-977 7, 512 Furo[3,2-6]pyri dines C NMR, 4, 982 synthesis, 4, 648, 981 Furo[c]pyri dines HMO data, 4, 976 Furo[2,3-c]pyri dines synthesis, 4, 977 Furo[3,2-c]pyri dines nitration, 4, 983 synthesis, 4, 978-981 Furo[3,4-c]pyri dines synthesis, 4, 982 Furo[3,2-c]pyridin-3-ols synthesis, 4, 980 Furo[2,3-6]pyridin-6-ones synthesis, 4, 976 Furo[3,4-c]pyridin-4-ones synthesis, 4, 982... [Pg.637]

General Procedure for the Silylformaltion/Sakurai Allylation. Synthesis of Polyol Fragments for Polyketide and Macrolide Synthesis. In a magnetically stirred stainless-steel Parr bomb the substrate (1 eq) is dissolved in benzene. The solution is cooled to - 78 °C until frozen. Rh(acac)(CO)2 (3 mol %) is then added and the Parr bomb is assembled and pressurized with CO (60 bar) and vented. This purge is repeated twice and the Parr bomb is pressurized with CO (60 bar) at - 78 °C. The apparatus is then immersed in an oil bath and heated at 60 °C for 22-24 h. After cooling to 0 °C, the bomb is vented. The solution... [Pg.89]

Salinosporamide synthesis 196 Sharpless asymmetric dihydroxylation (see also Osmylation) 84,89, 141, 189 Sharpless asymmetric epoxidation 32,141 Silane, allylic synthesis 43 Sonogashira coupling (see Pd)... [Pg.113]


See other pages where Synthesis allylic is mentioned: [Pg.61]    [Pg.51]    [Pg.51]   
See also in sourсe #XX -- [ Pg.455 , Pg.478 ]




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5-Allyl thiolates, synthesis

7-Alkoxy allylic stannanes synthesis

Acyclic stereoselective synthesis allyl metal reagents

Alkaloid syntheses allylation

Alkanes, 1,1-disulfinylreaction with allylic epoxides synthesis of macrolides

Alkanoic acid, 2-oxoesters synthesis, allylic anions

Alkenyl-allyl cross-coupling synthesis

Allyl acetates cyclic ether synthesis

Allyl acetates synthesis

Allyl acid-catalyzed synthesis

Allyl alcohols 1.3- diene synthesis

Allyl alcohols nitrile synthesis

Allyl alcohols, asymmetric synthesis

Allyl alcohols, nitroenantiomers synthesis

Allyl alcohols, synthesis

Allyl amides , oxazoline synthesis

Allyl carbonates nitrile synthesis

Allyl carbonates synthesis

Allyl chloride synthesis

Allyl complexes synthesis

Allyl cyanide synthesis

Allyl ether synthesis

Allyl glycosides, syntheses

Allyl halides, Grignard syntheses

Allyl hydrazines, synthesis

Allyl isocyanide synthesis

Allyl isothiocyanate, synthesis

Allyl phosphoryl compounds synthesis

Allyl silanes synthesis

Allyl silyl ethers synthesis

Allyl sulfonamides, synthesis

Allyl sulfoxide anions synthesis

Allyl sulphoxides synthesis

Allyl synthesis

Allyl synthesis

Allylic alcohol synthesis from aldol reactions

Allylic alcohols chiral hydroperoxide synthesis

Allylic alcohols prostaglandin synthesis

Allylic alcohols synthesis

Allylic alcohols, synthesis from

Allylic alcohols, synthesis from compounds

Allylic alcohols, synthesis from epoxides

Allylic alkylation synthesis

Allylic amides synthesis

Allylic amines synthesis

Allylic chlorides, synthesis

Allylic dactylolide synthesis

Allylic derivatives heterocyclic synthesis

Allylic derivatives natural products synthesis

Allylic derivatives tetrahydrofuran synthesis

Allylic halides synthesis

Allylic hydroperoxides natural product synthesis

Allylic hydroperoxides synthesis

Allylic iodides synthesis

Allylic peroxides, synthesis

Allylic polyprenols synthesis

Allylic silanes, synthesis

Allylic sulfonyl carbanions synthesis

Allylic sulfoximines synthesis

Allylic sulphones, synthesis

Allylic syntheses with

Amines allylic amine synthesis

Asymmetric Synthesis of Unsymmetrical Allylic Alcohols

Asymmetric synthesis allyl organometallics

Asymmetric synthesis allylation

Asymmetric synthesis allylic alkylation

Catalytic Asymmetric Synthesis Sharpless Oxidations of Allylic alcohols

Collins allylic oxidation in -dictyolene synthesis

Cyclopentenone synthesis allylic compounds

Diastereoselective synthesis monosubstituted allylic

Enantioselective synthesis Tsuji allylation

Enantioselective synthesis allylation

Enantioselective synthesis radical allylation

Epoxy allylic ether synthesis

Ethers, allyl vinyl ether synthesis

Ethers, allyl vinyl synthesis

Industrial synthesis allyl chloride

Ketones allylation-oxidations, 1,4-diketone synthesis, palladium

Ketones, allyl vinyl synthesis

Lactones synthesis, carbonylation of allylic alcohols

Ligand synthesis asymmetric allylation

Natural product synthesis allyl acetate

Natural product synthesis palladium-catalyzed allylation

Organozinc reagents, allylic synthesis

Primary amines allylic amine synthesis

Secondary amines allylic amine synthesis

Selected Applications of the Catalytic Enantioselective Allylation Reaction in Natural Product Synthesis

Selenides, allyl synthesis

Silane, allylic synthesis

Silanes, allyl cycloaddition reactions synthesis

Sodium bis aluminum hydride allylic alcohol synthesis

Stereoselective synthesis allyl organometallics

Stoichiometric synthesis allylation reactions

Sulfides, allyl synthesis

Sulfones, allyl dienyl synthesis

Sulfoxides, allylic synthesis

Synthesis Using Palladium Allyl Chemistry

Synthesis allylic oxidation

Synthesis and Characterization of Allyl-Functionalized Octa-Arm PIB Stars

Synthesis of Allylic Alcohols

Synthesis of Allylic Sulfides

Synthesis of Biologically Active Compounds via Allylic Substitution

Synthesis of Metal Complexes Containing Chelated Allyl Ligands

Synthesis of the Allyl Ethers

Synthesis reaction with allylic halides

The synthesis of non-racemic allylic alcohols

Xanthates, allylic synthesis

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