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(3R,4S,5R)-3-Bromo-5-((1S,2R)-1,2-dihydroxy-3-phenyl-penta-3,4-dienyl)-4-hydroxy-dihydro-furan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

204838-69-7

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204838-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204838-69-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,8,3 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 204838-69:
(8*2)+(7*0)+(6*4)+(5*8)+(4*3)+(3*8)+(2*6)+(1*9)=137
137 % 10 = 7
So 204838-69-7 is a valid CAS Registry Number.

204838-69-7Downstream Products

204838-69-7Relevant academic research and scientific papers

Indium-mediated highly diastereoselective allenylation in aqueous medium: Total synthesis of (+)-goniofufurone

Yi, Xiang-Hui,Meng, Yue,Li, Chao-Jun

, p. 449 - 450 (1998)

(+)-Goniofufurone was synthesized from D-glucurono-6,3-lactone via an indium-mediated highly regio- and diastereo-selective allenylation of carbonyl compounds in aqueous medium.

Regio- and diastereoselective allenylation of aldehydes in aqueous media: Total synthesis of (+)-goniofufurone

Yi, Xiang-Hui,Meng, Yue,Hua, Xiao-Gang,Li, Chao-Jun

, p. 7472 - 7480 (2007/10/03)

The regio- and diastereoselectivities of metal-mediated allenylation of carbonyl compounds were investigated in aqueous media. Different metal mediators showed varied regioselectivities on product formation during propargylation-allenylation reactions of carbonyl compounds with simple propargyl bromide. Under the standard reaction conditions, the use of indium provided the highest regioselectivity, with a preference of formation of the homopropargyl alcohol. The use of tin and bismuth as the metal mediator provided slightly lower selectivities with the same preference. The use of zinc and cadmium as the mediators further lowered the product selectivity. The reactions of an alipathic aldehyde with simple propargyl bromide showed a lower selectivity than the reaction of an aromatic aldehyde in most cases, except for the use of tin or zinc (where comparable selectivities were observed). On the other hand, the reaction of terminal-substituted propargyl bromides with aldehydes mediated by indium showed a high regioselectivity in forming allenylation products. The indium-mediated allenylation of carbonyl compounds bearing an α-hydroxyl group also proceeded with a high diastereoselectivity, forming syn-diols predominantly in aqueous ethanol. The high diastereoselectivity in allenylation of α-hydroxyl-substituted aldehydes was attributed to the chelation effect exhibited by the α-hydroxyl substituent. Through the use of this highly diastereoselective allenylation, (+)-goniofufurone was synthesized from D'-glucurono-6,3-lactone.

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