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4-Nonenoic acid, 7-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-9-[(4-methoxyphenyl)methoxy]-4, 6,8-trimethyl-, 2,6-dimethylphenyl ester, (4Z,6S,7R,8S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

261968-07-4

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261968-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 261968-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,1,9,6 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 261968-07:
(8*2)+(7*6)+(6*1)+(5*9)+(4*6)+(3*8)+(2*0)+(1*7)=164
164 % 10 = 4
So 261968-07-4 is a valid CAS Registry Number.

261968-07-4Relevant academic research and scientific papers

Synthesis of (Z)-Trisubstituted olefins by decarboxylative Grob-Type fragmentations: Epothilone D, discodermolide, and peloruside A

Prantz, Kathrin,Mulzer, Johann

experimental part, p. 485 - 506 (2010/06/14)

Methyl-branched (Z)-trisubstituted olefins are found in many polyketides with interesting biological activity, such as epothilone D (1), discodermolide (3), and peloruside A (2). Despite the employment of numerous different strategies, this motif has often been the weak point in total synthesis. Thus, we present a novel hydroxideinduced Grob-type fragmentation as an easy access to trisubstituted olefins. In our case, β-mesyloxy δ-lactones with three stereogenic centers were chosen whose fragmentation underlies a high stereoelectronic control. Major challenges in the syntheses were the instailation of quaternary stereocenters, achieved by enzymatic desymmetrization of meso-diesters and by aluminiumpromoted stereoselective rearrangement of chiral epoxides, respectively. Different aldol strategies were developed for the formation of the fragmentation precursors. Additionally a short survey about nucleophilic additions to aldehydes with quaternary α-centers is presented.

A second-generation total synthesis of (+)-discodermolide: The development of a practical route using solely substrate-based stereocontrol

Paterson, Ian,Delgado, Oscar,Florence, Gordon J.,Lyothier, Isabelle,O'Brien, Matthew,Scott, Jeremy P.,Sereinig, Natascha

, p. 150 - 160 (2007/10/03)

(Chemical Equation Presented). A novel total synthesis of the complex polyketide (+)-discodermolide, a promising anticancer agent of sponge origin, has been completed in 7.8% overall yield over 24 linear steps, with 35 steps altogether. This second-genera

A practical synthesis of (+)-discodermolide and analogues: Fragment union by complex aldol reactions

Paterson,Florence,Gerlach,Scott,Sereinig

, p. 9535 - 9544 (2007/10/03)

A practical stereocontrolled synthesis of (+)-discodermolide (1) has been completed in 10.3% overall yield (23 steps longest linear sequence). The absolute stereochemistry of the C1-C6 (7), C9-C16 (8), and Csub

Total synthesis of the antimicrotubule agent (+)-discodermolide using boron-mediated aldol reactions of chiral ketones

Paterson, Ian,Florence, Gordon J.,Gerlach, Kai,Scott, Jeremy P.

, p. 377 - 380 (2007/10/03)

With a similar mechanism of action to taxol, the title compound 1 is a particularly promising candidate for development in cancer chemotherapy. This efficient synthesis, based on stereocontrolled aldol reactions, should help to overcome the scarce natural

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