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(4S,5R)-3-(3-acetoxy-4-benzyloxyphenyl)-2-(benzyloxycarbonylmethylamino)-3-hydroxypropionic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

821006-85-3

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821006-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 821006-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,1,0,0 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 821006-85:
(8*8)+(7*2)+(6*1)+(5*0)+(4*0)+(3*6)+(2*8)+(1*5)=123
123 % 10 = 3
So 821006-85-3 is a valid CAS Registry Number.

821006-85-3Relevant academic research and scientific papers

Evolution of the total syntheses of ustiloxin natural products and their analogues

Li, Pixu,Evans, Cory D.,Wu, Yongzhong,Cao, Bin,Hamel, Ernest,Joullie, Madeleine M.

, p. 2351 - 2364 (2008/09/20)

Ustiloxins A-F are antimitotic heterodetic cyclopeptides containing a 13-membered cyclic core structure with a synthetically challenging chiral tertiary alkyl-aryl ether linkage. The first total synthesis of ustiloxin D was achieved in 31 linear steps using an SNAr reaction. An NOE study of this synthetic product showed that ustiloxin D existed as a single atropisomer. Subsequently, highly concise and convergent syntheses of ustiloxins D and F were developed by utilizing a newly discovered ethynyl aziridine ring-opening reaction in a longest linear sequence of 15 steps. The approach was further optimized to achieve a better macrolactamization strategy. Ustiloxins D, F, and eight analogues (14-MeO-ustiloxin D, four analogues with different amino acid residues at the C-6 position, and three (9R,10S)-epi-ustiloxin analogues) were prepared via the second-generation route. Evaluation of these compounds as inhibitors of tubulin polymerization demonstrated that variation at the C-6 position is tolerated to a certain extent. In contrast, the S configuration of the C-9 methylamino group and a free phenolic hydroxyl group are essential for inhibition of tubulin polymerization.

Total synthesis of ustiloxin D and considerations on the origin of selectivity of the asymmetric allylic alkylation

Sawayama, Andrew M.,Tanaka, Hiroko,Wandless, Thomas J.

, p. 8810 - 8820 (2007/10/03)

As part of investigations into cell cycle checkpoint inhibitors, an asymmetric synthesis of the antimitotic natural product, ustiloxin D, has been completed. A salen-Al-catalyzed aldol reaction was employed to construct a chiral oxazoline 9 (99% yield, 98

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