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1,7-Dioxaspiro[5.5]undecane, 3-methyl-2-[(1R)-1-methyl-2-(phenylsulfonyl)ethyl]-, (2S,3R,6S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93635-20-2

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93635-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93635-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,3 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93635-20:
(7*9)+(6*3)+(5*6)+(4*3)+(3*5)+(2*2)+(1*0)=142
142 % 10 = 2
So 93635-20-2 is a valid CAS Registry Number.

93635-20-2Upstream product

93635-20-2Relevant academic research and scientific papers

Synthesis of the C28 through C38 segment of okadaic acid using vinylogous urethane aldol chemistry: Part IV

Dankwardt, John W.,Dankwardt, Sharon M.,Schlessinger, Richard H.

, p. 4983 - 4986 (2007/10/03)

The synthesis of the C-28 through C-38 segment of the marine natural product okadaic acid was accomplished employing a highly enantio- and diasteroselective aldol condensation reaction of a chiral vinylogous urethane enolate. The stereocenter at C-29 was addressed utilizing a diastereoselective hydroboration reaction.

Synthesis of Okadaic Acid-Tautomycin Hybrid

Tsuboi, Katsunori,Ichikawa, Yoshiyasu,Isobe, Minoru

, p. 713 - 715 (2007/10/03)

One of the three spiro-segments in the synthesis of okadaic acid was synthesized under a new heteroconjugate addition strategy. Successive coupling of this spiro-segment with two tautomycin-synthetic segments afforded a hybrid molecule between okadaic acid and tautomycin.

SYNTHESIS OF A MARINE POLYETHER TOXIN, OKADAIC ACID (3). SYNTHESIS OF SEGMENT C.

Ichikawa, Yoshiyasu,Isobe, Minoru,Masaki, Hisanoru,Kawai, Takatoshi,Goto, Toshio,Katayama, Chuji

, p. 4759 - 4766 (2007/10/02)

The title compound was divided into three retrosynthetic segments, A, B and C, by disconnecting two C-C bonds at C-14/15 and C-27/28.Synthesis of the segment C in the optically active natural form starting from a D-glucose derivatives is described.The key

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