An Unusual C[dbnd]C Bond Cleavage with Chromium VI Reagents: Oxidation of Primary Alcohols to Ketones

Bijoy, P.; Rao, G. Sasibhushana

doi:10.1080/00397919308013800

Cited by 11 publications

(3 citation statements)

References 3 publications

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“…Oxidation of [G-1]-CH 2 OH with pyridinium dichromate (PDC) [38] in CH 2 Cl 2 gave the aldehyde [G-1]-CHO (1) in 75 % yield, which was transformed to the dibromo olefin [G-1]-CHCBr 2 (2) (96 %). Finally, elimination with lithium diisopropylamide (LDA) gave the first generation dendrimer alkyne [G-1]-C 2 H (3) in 75 % yield.…”

Section: Resultsmentioning

confidence: 99%

End-Cap Stabilized Oligoynes: Model Compounds for the Linear sp Carbon Allotrope Carbyne

et al. 2002

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Section: Resultsmentioning

confidence: 99%

End-Cap Stabilized Oligoynes: Model Compounds for the Linear sp Carbon Allotrope Carbyne

et al. 2002

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“…[2] The oxidation of primary alcohols to aldehydes can be accomplished with pyridinium dichromate (PDC) in CH 2 Cl 2 , [3] however, the reaction rate decreases and additional PDC reagent (above the 1.5 molar equivalents recommended) is often required. [4] Although general improvements have been made such as the addition of celite, [5] molecular sieves, [4,6,7] dry acetic acid, [6,7] or acetic anhydride, [8] these additions are not suitable for the partial oxidation of three-to five-carbon symmetrical diols, monoprotected as THP ethers, because of cleavage of THP ethers (presence of acid) and overoxidation to carboxylic acids.…”

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confidence: 98%

“…[5] The use of either freshly-activated molecular sieves or celite resulted in a significant amount (ca. 10%) of carboxylic acid formation (results observed in this laboratory).…”

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confidence: 99%

Oxidation of Monotetrahydropyranylated Short-Chain Symmetrical Diols

Petroski

2003

Synthetic Communications

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The free hydroxyl functions of monotetrahydropyranylated three-to five-carbon symmetrical primary diols are oxidized to aldehydes, without cleavage of the protective group, by using pyridinium dichromate in CH 2 Cl 2 and anhydrous MgSO 4 as a water scavenger. The oxidation procedure is improved for these specific compounds since over oxidation to carboxylic acids and formation of dimeric esters are suppressed.

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The Oxidation of Alcohols by Modified Oxochromium( VI )–Amine Reagents

Luzzio

1998

Organic Reactions

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The development of oxochromium(VI)‐amine reagents as oxidants in organic synthesis has evolved since the early studies of Sisler which described the use of adducts of heterocyclic nitrogen bases and chromium(VI) oxide. The later work of Sarrett and coworkers in steroid synthesis soon established the utility of chromium(VI) oxide‐pyridine adducts as the first selective oxochromium(VI)‐amine reagents. Several modifications of the Sarrett oxidation followed. The present concern with the toxicity and environmental implications of oxochromium(VI) has provided encouragement for the study and use of catalytic oxochromium reagents in conjunction with stoichiometric co‐oxidants such as peroxides. Such technology is welcome, particularly when applied to the large‐scale preparations found in industry where the disposal of byproducts is a constant problem. Modified oxochromium(VI)‐amine reagents on polymer supports have been prepared and examined with the objective of providing a regenerable reagent system which is serviceable on a practical scale. A significant improvement in routine oxidations utilizing PCC and PDC entails the addition of adsorbents such as Celite®, alumina, silica gel, molecular sieves, or zeolites. The distinct advantages associated with the use of adsorbents in oxochromium(VI)‐amine‐mediated oxidations are discussed. The importance of buffers and desiccants in oxochromium(VI) oxidations is discussed. Virtually any number of oxochromium(VI)‐amine reagents may be prepared by varying the amine ligand and/or acid species associated with oxochromium(VI), and many of these compounds have been tested using simple substrate alcohols for oxidation to carbonyl compounds. The search for a milder and more efficient oxidant than the Sarrett‐type oxochromium(VI) reagent systems as well as the nonchromium oxidants based on dimethyl sulfoxide or dimethyl sulfide led to an examination of the utility of pyridinium chlorochromate (PCC) in selective oxidations of alcohols. PCC was superior in terms of ease of preparation, shelf stability and economy. Since the introduction of PCC in 1975 the reagent has become a commercially available “textbook” compound and is usually the reagent of choice for routine large and small scale oxidations of alcohols to carbonyl compounds. Unlike the oxochromium(VI)‐pyridine adducts, PCC is an acid salt, and its properties have proven advantageous in a number of tandem oxidative reactions such as oxidative transpositions and oxidative cationic cyclizations. Several reviews address the versatility of PCC and its extension to many different types of oxidative conversions in single and multistep organic syntheses. While PCC was gaining widespread use, the utility of pyridinium dichromate (PDC) in solvents such as dimethylformamide (DMF) and dichloromethane was reported. PDC/DMF was useful for oxidizing allylic alcohols to the corresponding, α,β‐unsaturated carbonyl compounds and non‐conjugated aldehydes and primary alcohols to the corresponding carboxylic acids. The utilization of beyond the simple oxidation of alcohols, and it is now employed for various transformations. Many other types of substituted pyridines, nitrogen heterocycles and amines form chromates, dichromates, and chlorochromates which allow many different types of oxidative processes for a wide range of substrate molecules. This chapter surveys the many applications of oxochromium(VI) complexes in oxidative conversions of alcohols to carbonyl compounds. Alternative reagent systems based on modifications involving ligands, buffering agents, or adsorbents, as well as nonchromium(VI) oxidants are discussed. A variety of substrates have been included in the Tables so as to guide the synthetic chemist in selecting reagents and conditions that will be optimal for a given transformation. Oxidative conversions of alcohols through transpositions and cationic cyclizations giving carbonyl compounds as endproducts are included.

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An Unusual C[dbnd]C Bond Cleavage with Chromium VI Reagents: Oxidation of Primary Alcohols to Ketones

Cited by 11 publications

References 3 publications

End-Cap Stabilized Oligoynes: Model Compounds for the Linear sp Carbon Allotrope Carbyne

End-Cap Stabilized Oligoynes: Model Compounds for the Linear sp Carbon Allotrope Carbyne

Oxidation of Monotetrahydropyranylated Short-Chain Symmetrical Diols

The Oxidation of Alcohols by Modified Oxochromium( VI )–Amine Reagents

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