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(2'R,4'R,6'R)-3''-{6'-[2-(4-methoxybenzyloxymethyl)-oxazol-4-yl]-4'-(triisopropylsilanyloxy)-tetrahydropyran-2'-yl}-propane-1'',2''-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

265666-21-5

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  • (2'R,4'R,6'R)-3''-{6'-[2-(4-methoxybenzyloxymethyl)-oxazol-4-yl]-4'-(triisopropylsilanyloxy)-tetrahydropyran-2'-yl}-propane-1'',2''-diol

    Cas No: 265666-21-5

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  • (2'R,4'R,6'R)-3''-{6'-[2-(4-methoxybenzyloxymethyl)-oxazol-4-yl]-4'-(triisopropylsilanyloxy)-tetrahydropyran-2'-yl}-propane-1'',2''-diol

    Cas No: 265666-21-5

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265666-21-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 265666-21-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,5,6,6 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 265666-21:
(8*2)+(7*6)+(6*5)+(5*6)+(4*6)+(3*6)+(2*2)+(1*1)=165
165 % 10 = 5
So 265666-21-5 is a valid CAS Registry Number.

265666-21-5Upstream product

265666-21-5Relevant articles and documents

Total synthesis of (+)-phorboxazole A, a potent cytostatic agent from the sponge Phorbas sp.

Pattenden, Gerald,Gonzalez, Miguel A,Little, Paul B,Millan, David S,Plowright, Alleyn T,Tornos, James A,Ye, Tao

, p. 4173 - 4208 (2007/10/03)

A convergent total synthesis of phorboxazole A (1a), from the C(3-19), C(20-27) and C(33-46) fragments 5, 4 and 91, respectively, concentrating on stereocontrolled formation of the bonds at C(2-3), C(19-20) and C(27-28), is described. Although a coupling reaction between a macrolide ketone and the side chain substituted sulfone, at C(27-28) was not successful, a Wadsworth-Emmons olefination involving the oxane methyl ketone 4 and an oxazole produced the oxane 90 which was next coupled to 91 leading to the C(20-46) unit 100. A further coupling of 100 to 71c at C(19-20) then led to 105, ultimately, and the synthesis was completed by a macrocyclisation reaction from 105, at the C(2-3) alkene bond, followed by deprotection of 106.

Synthetic studies towards phorboxazole A. Stereoselective synthesis of the C3-C19 bis-oxane oxazole portion of the phorboxazole macrolide

Pattenden, Gerald,Plowright, Alleyn T.

, p. 983 - 986 (2007/10/03)

A synthesis of the C3-C19 bis-oxane portion of phorboxazole A, involving an oxy anion intramolecular Michael reaction to produce a cis-oxane and an intramolecular Williamson reaction leading to a trans-oxane, is described. (C) 2000 Elsevier Science Ltd.

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