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(4R,5S)-5-tert-Butyl-4-(1-iodo-vinyl)-3-(toluene-4-sulfonyl)-oxazolidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137764-92-2

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137764-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137764-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,7,6 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 137764-92:
(8*1)+(7*3)+(6*7)+(5*7)+(4*6)+(3*4)+(2*9)+(1*2)=162
162 % 10 = 2
So 137764-92-2 is a valid CAS Registry Number.

137764-92-2Relevant academic research and scientific papers

A highly stereoselective preparation of syn-1,2-diols from secondary α-allenic alcohols via iodocyclization. Synthesis of (±)-threo-L-factor and (±)-disparlure

Friesen,Giroux

, p. 1857 - 1865 (2007/10/02)

The iodocyclization of the N-tosyl carbamates 5 of secondary α-allenic alcohols 4 is described. The reaction sequence involves the addition of iodine to the terminal olefin of the allene moiety of 5 resulting in the formation of an isomeric mixture of Z and E diiodides 6 and 7. This initial process is followed, in the same pot, by reaction of the diiodides with silver carbonate. Hydrolysis of the resulting trans imino carbonates 8 provides syn-1,2-diols 10 in highly diastereoselective (>50:1) and regioselective (>20:1) fashion. Oxazolidinones 9 are minor products that arise from the participation of the carbamate nitrogen atom in the cyclization reaction. The regioselectivity of the cyclization reaction from 6/7 to 8 is highly dependent upon the reaction solvent with the optimum results being obtained in ether/MeCN mixtures (10:1 to 50:1) or CH2Cl2. The synthetic utility of the vinyl iodo diols 10 is demonstrated by the synthesis of (±)-threo-5-hydroxy-4-decanolide (17) ((±)-threo-L-factor) and (±)-cis-7,8-epoxy-2-methyloctadecane (24) ((±)-disparlure). The key step in each synthesis involves the conversion of the vinyl iodide moiety of 10 into the alkynes 15 or 18 (from 10j and 10k, respectively) via a high-yielding dehydrohalogenation reaction.

Enantioselective Route to α-Hydroxy Aldehyde and Acid Derivatives

Corey, E. J.,Jones, Graham B.

, p. 5713 - 5716 (2007/10/02)

Methodology is described for the enantioselective synthesis of chiral O-protected α-hydroxy aldehydes, acids and esters from achiral aldehydes having one less carbon.

Iodocyclization of the (Tolylsulfonyl)- and (Trichloroacetyl)carbamates of Secondary α-Allenic Alcohols. Highly Diastereoselective Synthesis of syn-1,2-Amino Alcohols and trans-5-Alkyl-1-oxo-2-oxazolidine-4-carboxylic Acids

Friesen, Richard W.,Kolaczewska, Aleksandra E.

, p. 4888 - 4895 (2007/10/02)

The iodocyclization of tosyl- and (trichloroacetyl)carbamates 9 and 10, respectively, of secondary α-allenic alcohols is described.The cyclofunctionalization reactions are highly diastereoselective, providing trans-5-alkyl-4-(1-iodoethylene)-2-oxazolidino

A HIGHLY STEREOSELECTIVE CONVERSION OF α-ALLENIC ALCOHOLS TO 1,2-SYN AMINO ALCOHOL DERIVATIVES VIA IODOCARBAMATION

Friesen, Richard W.

, p. 4249 - 4252 (2007/10/02)

The iodocarbamation of α-allenic alcohol O-carbamates is described.Reactions carried out in anhydrous Et2O are highly diastereoselective, providing the cyclic carbamates trans-8 and cis-9 in ratios ranging from 21:1 to >99:1.Hydrolysis and acetylation pr

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