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(3S,8aS)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-hexahydro-indolizine-5,8-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

181705-73-7

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181705-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 181705-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,7,0 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 181705-73:
(8*1)+(7*8)+(6*1)+(5*7)+(4*0)+(3*5)+(2*7)+(1*3)=137
137 % 10 = 7
So 181705-73-7 is a valid CAS Registry Number.

181705-73-7Downstream Products

181705-73-7Relevant academic research and scientific papers

Total synthesis of (-)-sessilifoliamide J

Liu, Xue-Kui,Ye, Jian-Liang,Ruan, Yuan-Ping,Li, Yu-Xiu,Huang, Pei-Qiang

, p. 35 - 41 (2013/04/10)

An efficient synthesis of the Stemona alkaloid (-)-sessilifoliamide J (1) in 12 steps and 7.7% overall yield from the known building block 8 is presented. The synthesis features the Corey lactonization reaction and a highly diastereoselective α-methylation reaction to build the spirolactone moiety.

Towards stereochemical control: Two approaches for the highly anti-diastereoselective construction of the spirolactone moieties of some Stemona alkaloids

Tuo, Shichuan,Liu, Xuekui,Huang, Peiqiang

, p. 55 - 62 (2013/08/24)

Some Stemona alkaloids belonging to the tuberostemospironine group possess a spirolactone moiety with anti-configuration (C-9/C-9a). In this paper, we describe two approaches to this structural unity. By using bromine atom as a traceless directing group, the SmI2-mediated reductive coupling of ketone 6 and β-bromomethacrylate proceeded with complete anti-diastereoselectivity. In the absence of an α-directing (chelation) group, the one-pot reaction of the ketone derived from alcohol 15 with the organozinc reagent generated from bromomethacrylate afforded spiro-α-methylene-γ-lactone derivative 16 as a single diastereomer. These two highly diastereoselective methods would find application in the synthesis of stemona alkaloids containing anti-configured spiro-lactone/ pyrrolidine moieties. In addition, on the basis of our previous work, the total synthesis of (-)-9-epi-11-demethylsessilifoliamide J (11), and an improved synthesis of (-)-9,11-di-epi-sessilifoliamide J (9) were accomplished. Completely anti-diastereoselective: This can be achieved by using bromine atom as a traceless directing group in the SmI2-mediated reductive coupling of α,β-unsaturated ester with ketones; or by the one-pot reaction of the organozinc reagent generated from bromomethacrylate with ketone. On the basis of these results, two approaches to the spirolactone moiety with anti-configuration (C-9/C-9a) found in some Stemona alkaloids were disclosed. Copyright

A versatile synthesis of a β-turn peptidomimetic scaffold: An approach towards a designed model antagonist of the tachykinin NK-2 receptor

Hanessian, Stephen,McNaughton-Smith, Grant

, p. 1567 - 1572 (2007/10/03)

A general and stereocontrolled synthesis of an azabicyclo[4.3.0]nonane amino acid template with an appended substitutent at C-5 was developed. The approach allows for stereochemical and functional variations that extend the utility of these rigid amino acid motifs as peptidomimetics. The synthesis of a weakly active but specific NK-2 receptor antagonist is described.

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