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(2R,3S,12bR)-methyl 1,2,3,4,6,7,12,12b-octahydro-4-oxo-2-phenylindolo[2,3-a]quinolizine-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1133909-62-2

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1133909-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1133909-62-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,3,9,0 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1133909-62:
(9*1)+(8*1)+(7*3)+(6*3)+(5*9)+(4*0)+(3*9)+(2*6)+(1*2)=142
142 % 10 = 2
So 1133909-62-2 is a valid CAS Registry Number.

1133909-62-2Downstream Products

1133909-62-2Relevant academic research and scientific papers

Diverse asymmetric quinolizidine synthesis: A stereodivergent one-pot approach

Zhanga, Wei,Franzena, Johan

supporting information; experimental part, p. 499 - 518 (2010/06/17)

A diverse stereodivergent organocatalytic one-pot addition/cyclization/ annulation sequence to optically active quinolizidine derivatives from easily available starting materials is presented. The one-pot sequence relies on a pyrrolidine-catalyzed enantioselective conjugate addition of electron-deficient amide a-carbons to α,β-unsaturated aldehydes, spontaneous hemiaminal formation and acid-catalyzed/mediated N-acyliminium ion cyclization to give the quinolizidine framework. Simple tuning of the reaction conditions in the N-acyliminuim ion cyclization step provides a diastereomeric switch, which gives access to both of the two bridgehead epimers through kinetic, thermodynamic or chelation control. The methodology display a broad substrate scope that is demonstrated by the stereoselective formation of indolo-, thieno-, benzofuro-, furo- and different benzoquinolizidine derivatives with high atom efficiency, up to >99% ee and up to >95:5 dr. Due to its efficiency, synthetic diversity and operational simplicity, this protocol has the potential to find important use as a key step in natural product synthesis, biochemistry and pharmaceutical science. The stereochemical outcome of the one-pot sequence was investigated, and the mechanism and origin of stereoselectivity of the different steps is discussed.

Diastereoselective syntheses of indoloquinolizidines by a pictet-spengler/lactamization cascade

Fang, Huihui,Wu, Xiaoyu,Nie, Linlin,Dai, Xiaoyang,Chen, Jie,Cao, Weiguo,Zhao, Gang

, p. 5366 - 5369 (2011/03/19)

An expedient diastereoselective synthesis of highly functionalized indolo[2,3-α]quinolizidines adopting a cis H2/H12b geometry has been realized by a Pictet-Spengler/lactamization cascade sequence. The absolute stereochemistry at C2, C3, and C12b was gove

Asymmetric alkaloid synthesis: A one-pot organocatalytic reaction to quinolizidine derivatives

Franzen, Johan,Fisher, Andreas

supporting information; experimental part, p. 787 - 791 (2009/05/06)

(Chemical Equation Presented) One pot+two steps = three stereocenters: A short enantioselective synthesis to access the indolo[2,3a]quinolizidine and the benzo[a]quinolizidine skeleton has been developed (see scheme; TMS = trimethylsilyl, R1 =

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