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1H-2,1,3-Benzothiadiazin-4(3H)-one, 3-(1-methylethyl)-, 2,2-dioxide

Kamm, O., Segur, J. B. 2003. Methyl m-Nitrobenzoate. Organic Syntheses. 71.

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Phenol, 2-(2H-benzotriazol-2-yl)-4,6-bis(1,1-dimethylpropyl)-

Sharpless, Syntheses and Crystal Structures of the Cinchona Alkaloid Derivatives used as Ligands in the Osmium-Catalyzed Asymmetric Dihydroxylation of Olefins,

Sharpless, Catalytic Asymmetric Synthesis of New Halogenated Chiral Synthons, , 3, 517 (1997).

Zargarian, Synthesis of Optically Active Secondary Allylic Alcohols from Allylsilanes via Successive Asymmetric Dihydroxylation (AD) and Peterson Olefination Reactions, , 34, 2509 (1993

1,4-Cyclohexanedimethanol, dibenzoate

Sharpless, Syntheses of Diols by Catalytic Dihydroxylation Reactions, "Applied Homogeneous Catalysis by Organometallic Complexes", Boy Cornils and Wolfgang A.

Sharpless, Enantioselective Synthesis of Both Enantiomers of 7,7-Dimethyl-6,8-dioxabicyclo-[3.2.1]octane via Regioselective Asymmetric Dihydroxylation, , 1, 47 (1993) .

2-Benzothiazolesulfenamide, N-(1,1-dimethylethyl)-

Fokin, Rapid Discovery and Structure-Activity Profiling of Novel Inhibitors of HIV-1 Protease Enabled by the Copper(I)-Catalyzed Synthesis of 1,2,3-Triazoles and Their Further Functionalization,

Sharpless, Asymmetric Dihydroxylation of Acrolein Acetals: Synthesis of Stable Equivalents of Enantiopure Glyceraldehyde and Glycidaldehyde, , 33, 2095 (1992).

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  • Phenol, 2-(2H-benzotriazol-2-yl)-4,6-bis(1,1-dimethylethyl)-

    Methyl 3-Nitrobenzoate

  • Thiocyanic acid, (2-benzothiazolylthio)methyl ester

    Sharpless, A Simple and Efficient Method for the Preparation of Pyridine--oxides II, , 39, 761 (1998).

  • 1H-Benzotriazole, 4(or 5)-methyl-

    Sharpless, Enantioselective Synthesis of Juvenile Hormone III in Three Steps from Methyl Farnesoate, , 8, 777 (1993).

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Phenol, 2-(2H-benzotriazol-2-yl)-4,6-bis(1-methyl-1-phenylethyl)-

1. Draw all resonance structures for the nitration of methyl benzoate occurring at the ortho, meta, and para positions. Be sure to include all charges.

1H-Benzotriazole-1-methanamine, N,N-bis(2-ethylhexyl)-4-methyl-

Bring a clean, dry 25 x 150 mm test tube to the storeroom manager and trade it in for a 6.2 mL (6.8 g, 0.050 moles) sample of methyl benzoate (weigh the sample before you begin to obtain an exact weight). Place 14.5 mL (26.7 g) of concentrated sulfuric acid in a 125 rnL Erlenmeyer flask, cool it to 0 °C in an ice/water bath, then add all of the methyl benzoate with swirling.

1H-Benzotriazole-1-methanamine, N,N-bis(2-ethylhexyl)-5-methyl-

Sharpless, Asymmetric Epoxidation Provides Shortest Routes to Four Chiral Epoxy Alcohols which are Key Intermediates in Syntheses of Methymycin, Erythromycin, Leukotriene C-1 and Disparlure,

1H-Benzotriazole-1-methanamine, N,N-bis(2-ethylhexyl)-ar-methyl-

In this experiment, you will synthesize methyl-m-nitrobenzoate from methyl benzoate via electrophilic aromatic substitution. The isolated product will be purified by recrystallization, and purity will be determined from the melting point.

Benzoic acid, 4-hydroxy-, phenylmethyl ester

L-Ascorbic acid, 2-[(2R)-3,4-dihydro-2,5,7,8-tetramethyl-2-[(4R,8R)-4,8,12-trimethyltridecyl]-2H-1-benzopyran-6-YL hydrogen phosphate], potassium salt (1:1)

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