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(2S,3R,5R,7S,8R)-2-Hydroxymethyl-7-(4-methoxy-benzyloxy)-3,5-dimethyl-8-(2-triisopropylsilanyloxy-ethyl)-oxocan-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

911237-17-7

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911237-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 911237-17-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,2,3 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 911237-17:
(8*9)+(7*1)+(6*1)+(5*2)+(4*3)+(3*7)+(2*1)+(1*7)=137
137 % 10 = 7
So 911237-17-7 is a valid CAS Registry Number.

911237-17-7Upstream product

911237-17-7Relevant academic research and scientific papers

Enantioselective total synthesis of brevetoxin A: Unified strategy for the B, E, G, and J subunits

Crimmins, Michael T.,Ellis, J. Michael,Emmitte, Kyle A.,Haile, Pamela A.,McDougall, Patrick J.,Parrish, Jonathan D.,Zuccarello, J. Lucas

supporting information; experimental part, p. 9223 - 9234 (2010/04/25)

Brevetoxin A is a decacyclic ladder toxin that possesses 5-, 6-, 7-, 8-, and 9-membered oxacycles, as well as 22 tetrahedral stereocenters. Herein, we describe a unified approach to the B, E, G, and J rings based upon a ring-closing metathesis strategy from the corresponding dienes. The enolate technologies developed in our laboratory allowed access to the precursor acyclic dienes for the B, E, and G medium-ring ethers. The strategies developed for the syntheses of these four monocycles ultimately provided multigram quantities of each of the rings, supporting our efforts toward the completion of a convergent synthesis of brevetoxin A.

Improved synthesis of the ABCDE fragment of brevetoxin A

Crimmins, Michael T.,McDougall, Patrick J.,Ellis, J. Michael

, p. 4079 - 4082 (2007/10/03)

A second-generation synthesis of the BCDE fragment of brevetoxin A is described. Novel reactions were developed that extend the utility of the asymmetric glycolate alkylation reaction and improve scale-up to provide gram quantities of the B and E subunits

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