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erythro-2-Diphenylphosphinoyl-1-phenylbutane-1,4-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89625-17-2

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89625-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89625-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,2 and 5 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89625-17:
(7*8)+(6*9)+(5*6)+(4*2)+(3*5)+(2*1)+(1*7)=172
172 % 10 = 2
So 89625-17-2 is a valid CAS Registry Number.

89625-17-2Relevant academic research and scientific papers

Diphenylphosphinoyl lactones in the control of remote stereochemistry

Mitchell, Helen J.,Warren, Stuart

, p. 2105 - 2108 (2007/10/03)

E-alkenes with three stereogenic centres related 1,4- and 1,5- across the double bond can be prepared with good stereoselectivity from 3-diphenylphosphinoyl-4-alkenyl butyrolactones by alkylation, epoxidation, epoxide opening by a nucleophile, reduction a

Stereochemically controlled Synthesis of Unsaturated Alcohols by the Horner-Wittig Reaction

Ayrey, Peter M.,Bolton, Michael A.,Buss, Antony D.,Greeves, Nicholas,Levin, Daniel,et al.

, p. 3407 - 3418 (2007/10/02)

Single isomers (E or Z) of unsaturated alcohols with two to five carbon atoms between the double bond and the OH group may be made by the phosphine oxide version of the Horner-Wittig reaction.Hydroxyalkyldiphenylphosphine oxides react with aldehydes either directly or as silyl ethers to give a moderately Z-selective synthesis, while rearrangement of esters of the same alcohols by acyl transfer or acylation of alkyldiphenylphosphine oxides with lactones gives hydroxy ketones whose reduction and elimination leads to an E-selective synthesis.In most cases, separation of the diastereoisomers of the Horner-Wittig intermediates leads to the preparation of pure E- or Z-alkenols.

ACYL TRANSFER REACTIONS WITH PHOSPHINE OXIDES: SYNTHESIS OF E-HOMOALLYLIC ALCOHOLS, CYCLOPROPYL KETONES, AND γ-HYDROXY KETONES

Wallace, Paul,Warren, Stuart

, p. 2971 - 2978 (2007/10/02)

Esters of 3-hydroxypropylphosphine oxides rearrange in base by O to C acyl (RCO) transfer to give the hydroxy ketones (8). threo-Selective reduction of (8) leads to pure E-homoallylic alcohols whilst C to O acyl )Ph2PO) transfer leads to γ-hydroxy ketones with nucleophilic aqueous base or cyclopropyl ketones with BuOKt - HOBut.

SYNTHESIS OF E-HOMOALLYLIC ALCOHOLS, γ-HYDROXYKETONES, AND CYCLOPROPYL KETONES FROM 3-DIPHENYLPHOSPHINOYL (Ph2PO) PROPANOLS BY ACYL TRANSFER

Wallace, Paul,Warren, Stuart

, p. 5713 - 5716 (2007/10/02)

Carboxyl transfer (O*C) on 3-Ph2PO propyl esters (9) gives an intermediate (10) from which the Ph2PO group may be removed by the Horner-Witting reaction or by Ph2PO transfer (C*O) to give the title compounds.

SYNTHESIS OF SINGLE ISOMERS (E OR Z) OF UNSATURATED ALCOHOLS BY THE HORNER-WITTIG REACTION

Buss, Antony D,Greeves, Nicholas,Levin, Daniel,Wallace, Paul,Warren, Stuart

, p. 357 - 360 (2007/10/02)

Single isomers (E or Z) of homoallylic and higher alcohols can be synthesised from ω-hydroxyalkyldiphenylphosphine oxides and aldehydes, or from alkyldiphenylphosphine oxides and lactones

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