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1,2-Cyclopentanediol, monoacetate, (1R,2S)-rel- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20520-68-7

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20520-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20520-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,2 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20520-68:
(7*2)+(6*0)+(5*5)+(4*2)+(3*0)+(2*6)+(1*8)=67
67 % 10 = 7
So 20520-68-7 is a valid CAS Registry Number.

20520-68-7Relevant academic research and scientific papers

A one-step procedure for the monoacylation of symmetrical 1,2-diols

Clarke, Paul A.,Kayaleh, Nadim E.,Smith, Martin A.,Baker, James R.,Bird, Stephan J.,Chan, Chuen

, p. 5226 - 5231 (2002)

A series of lanthanide (III) salts have been shown to catalyze the monoacylation of symmetrical 1,2-diols by carboxylic acid anhydrides with surprisingly high selectivity.

Regioselective lithiation of benzyl imidazole: Synthesis and evaluation of new organocatalysts for trans-diol functionalization.

El-Mansy, Mohamed,Ghosh, Ankan,Cheong, Paul Ha-Yeon,Carter, Rich

supporting information, p. 3131 - 3139 (2019/09/03)

Benzyl imidazole was successfully lithiated using n-BuLi at ?78 °C and verified by deuterium incorporation. The chemical reaction of the lithiated benzimidazole was explored with a series of different electrophiles. This approach was utilized to synthesiz

Macrocyclic proline derived HCV serine protease inhibitors

-

Page/Page column 137, (2016/01/20)

The present invention discloses compounds of Formula I or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit serine protease activity, particularly the activity of hepatitis C virus (HCV) NS3-NS4A protease. Consequently, the com

3-Deazaneplanocin A and neplanocin a analogues and their effects on apoptotic cell death

Tam, Eric K.W.,Nguyen, Tuan Minh,Lim, Cheryl Z.H.,Lee, Puay Leng,Li, Zhimei,Jiang, Xia,Santhanakrishnan, Sridhar,Tan, Tiong Wei,Goh, Yi Ling,Wong, Sze Yue,Yang, Haiyan,Ong, Esther H.Q.,Hill, Jeffrey,Yu, Qiang,Chai, Christina L.L.

supporting information, p. 173 - 182 (2015/04/14)

3-Deazaneplanocin A (DzNep) is a potential epigenetic drug for the treatment of various cancers. DzNep has been reported to deplete histone methylations, including oncogenic EZH2 complex, giving rise to epigenetic modifications that reactivate many silenced tumor suppressors in cancer cells. Despite its promise as an anticancer drug, little is known about the structure-activity relationships of DzNep in the context of epigenetic modifications and apoptosis induction. In this study, a number of analogues of DzNep were examined for DzNeplike ability to induce synergistic apoptosis in cancer cells in combination with trichostatin A, a known histone deacetylase (HDAC) inhibitor. The structure-activity relationship data thus obtained provide valuable information on the structural requirements for biological activity. The studies identified three compounds that show similar activities to DzNep. Two of these compounds show good pharmacokinetics and safety profiles. Attempts to correlate the observed synergistic apoptotic activities with measured S-adenosylhomocysteine hydrolase (SAHH) inhibitory activities suggest that the apoptotic activity of DzNep might not be directly due to its inhibition of SAHH.

Alcohol cross-coupling for the kinetic resolution of diols via oxidative esterification

Hofmann, Christine,Schümann, Jan M.,Schreiner, Peter R.

, p. 1972 - 1978 (2015/02/19)

We present an organocatalytic C-O-bond cross-coupling strategy to kinetically resolve racemic diols with aromatic and aliphatic alcohols, yielding enantioenriched esters. This one-pot protocol utilizes an oligopeptide multicatalyst, m-CPBA as the oxidant, and N,N-diisopropylcarbodiimide as the activating agent. Racemic acyclic diols as well as trans-cycloalkane-1,2-diols were kinetically resolved, achieving high selectivities and good yields for the products and recovered diols.

Enantiomerically enriched trans-diols from alkenes in one pot: A multicatalyst approach

Hrdina, Radim,Mueller, Christian E.,Wende, Raffael C.,Wanka, Lukas,Schreiner, Peter R.

supporting information; experimental part, p. 2498 - 2500 (2012/04/10)

Multicatalysts consisting of non-natural oligopeptides with distinctly different catalytic moieties create molecular complexity in a multistep one-pot sequence starting from simple alkenes yielding highly enantiomerically enriched trans-diols. The Royal Society of Chemistry 2012.

Metal-free, organocatalytic syn diacetoxylation of alkenes

Zhong, Wenhe,Liu, Shan,Yang, Jun,Meng, Xiangbao,Li, Zhongjun

supporting information; experimental part, p. 3336 - 3339 (2012/08/29)

A novel method for the organocatalytic syn diacetoxylation of alkenes has been developed using aryl iodides as efficient catalysts. A broad range of substrates, including electron-rich as well as electron-deficient alkenes, are smoothly transformed by the new procedure, furnishing the desired products in good to excellent yields with high diastereoselectivity (up to >19:1 dr).

Kinetic resolution of trans-cycloalkane-1,2-diols via Steglich esterification

Hrdina, Radim,Mueller, Christian E.,Schreiner, Peter R.

supporting information; experimental part, p. 2689 - 2690 (2010/07/08)

We describe the efficient and highly enantioselective kinetic resolution of trans-cycloalkane-1,2-diols utilizing an enantioselective Steglich reaction with a variety of carboxylic acids that form the corresponding anhydrides in situ.

One-Pot desymmetrization of meso-l,2-hydrocarbon diols through acylation and oxidation

Mueller, Christian E.,Zell, Daniela,Schreiner, Peter R.

supporting information; experimental part, p. 9647 - 9650 (2010/04/28)

Avoid racemization! Short lipophilic oligopeptides utilizing nucleophilic N-jt-methyl histidine residues catalyze the desymmetrization of wieso-l,2-diols with enantiomeric ratios of up to 94:6. Direct one-pot oxidation, which avoids the well-known racemiz

Enantioselective kinetic resolution of trans-cycloalkane-1,2-diols

Mueller, Christian E.,Wanka, Lukas,Jewell, Kevin,Schreiner, Peter R.

supporting information; experimental part, p. 6180 - 6183 (2009/04/06)

Finally! The title resolution is achieved with a nonnatural, partially rigid, lipophilic tetrapeptide at low catalyst loadings without additional base or cosolvents. The transition-state model (ball-and-stick model in the scheme; C gray, N blue, O red) emphasizes the interplay between hydrogen-bonding and hydrophobic interactions. (Chemical Equation Presented)

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