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(2R,6S)-2-(benzyloxymethyl)-6-(((2R,4S,6R)-4-(triisopropylsilyloxy)-6-(2-(triisopropylsilyloxy)methyl-1,3-oxazol-4-yl)tetrahydro-2H-pyran-2-yl)-methyl)-tetrahydro-4H-pyran-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

296795-41-0

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296795-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 296795-41-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,6,7,9 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 296795-41:
(8*2)+(7*9)+(6*6)+(5*7)+(4*9)+(3*5)+(2*4)+(1*1)=210
210 % 10 = 0
So 296795-41-0 is a valid CAS Registry Number.

296795-41-0Upstream product

296795-41-0Relevant academic research and scientific papers

Application of complex aldol reactions to the total synthesis of phorboxazole B

Evans,Fitch,Smith,Cee

, p. 10033 - 10046 (2007/10/03)

The synthesis of phorboxazole B has been accomplished in 27 linear steps and an overall yield of 12.6%. The absolute stereochemistry of the C4-C12, C33-C38, and C13-C19 fragments was established utilizing catalytic asymmetric aldol methodology, while the absolute stereochemistry of the C20-C32 fragment was derived from an auxiliary-based asymmetric aldol reaction. All remaining chirality was incorporated through internal asymmetric induction, with the exception of the C43 stereocenter which was derived from (R)-trityl glycidol. Key fragment couplings include a stereoselective double stereodifferentiating aldol reaction, a metalated oxazole alkylation, an oxazole-stabilized Wittig olefination, and a chelation-controlled addition of the fully elaborated alkenyl metal side chain.

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