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19,21-Epoxyaspidospermidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36459-35-5

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36459-35-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36459-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,4,5 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36459-35:
(7*3)+(6*6)+(5*4)+(4*5)+(3*9)+(2*3)+(1*5)=135
135 % 10 = 5
So 36459-35-5 is a valid CAS Registry Number.

36459-35-5Downstream Products

36459-35-5Relevant academic research and scientific papers

Enantioselective Total Syntheses of (+)-Fendleridine and (+)-Acetylaspidoalbidine

Ghosh, Arun K.,Born, Joshua R.,Kassekert, Luke A.

, p. 5167 - 5175 (2019/05/10)

Enantioselective syntheses of hexacyclic aspidoalbidine alkaloids (+)-fendleridine (2) and (+)-acetylaspidoalbidine (3) are described. These syntheses feature an asymmetric decarboxylative allylation and photocyclization of a highly substituted enaminone. Also, the synthesis highlights the formation of a C19-hemiaminal ether via a reduction/condensation/intramolecular cyclization cascade with the C21-alcohol. The present synthesis provides convenient access to the aspidoalbidine hexacyclic alkaloid family in an efficient manner.

Concise Total Syntheses of (+)-Haplocidine and (+)-Haplocine via Late-Stage Oxidation of (+)-Fendleridine Derivatives

White, Kolby L.,Movassaghi, Mohammad

, p. 11383 - 11389 (2016/11/01)

We report the first total syntheses of (+)-haplocidine and its N1-amide congener (+)-haplocine. Our concise synthesis of these alkaloids required the development of a late-stage and highly selective C-H oxidation of complex aspidosperma alkaloid derivatives. A versatile, amide-directed ortho-acetoxylation of indoline amides enabled our implementation of a unified strategy for late-stage diversification of hexacyclic C19-hemiaminal ether structures via oxidation of the corresponding pentacyclic C19-iminium ions. An electrophilic amide activation of a readily available C21-oxygenated lactam, followed by transannular cyclization and in situ trapping of a transiently formed C19-iminium ion, expediently provided access to hexacyclic C19-hemiaminal ether alkaloids (+)-fendleridine, (+)-acetylaspidoalbidine, and (+)-propionylaspidoalbidine. A highly effective enzymatic resolution of a non-β-branched primary alcohol (E = 22) allowed rapid preparation of both enantiomeric forms of a C21-oxygenated precursor for synthesis of these aspidosperma alkaloids. Our synthetic strategy provides succinct access to hexacyclic aspidosperma derivatives, including the antiproliferative alkaloid (+)-haplocidine.

Total synthesis of (+)-fendleridine (aspidoalbidine) and (+)-1 -acetylaspidoalbidine

Campbell, Erica L.,Zuhl, Andrea M.,Liu, Christopher M.,Boger, Dale L.

supporting information; experimental part, p. 3009 - 3012 (2010/04/30)

A total synthesis of the Aspidosperma alkaloids (+)-fendleridine and (+)-1-acetylaspidoalbidine is detailed, providing access to both enantiomers of the natural products and establishing their absolute configuration. Central to the synthetic approach is a

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