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5-Phenyl-3-methyl-pent-4-in-2-ensaeure-methylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91902-66-8

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91902-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91902-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,0 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91902-66:
(7*9)+(6*1)+(5*9)+(4*0)+(3*2)+(2*6)+(1*6)=138
138 % 10 = 8
So 91902-66-8 is a valid CAS Registry Number.

91902-66-8Downstream Products

91902-66-8Relevant academic research and scientific papers

Asymmetric synthesis of chiral β-alkynyl carbonyl and sulfonyl derivatives: Via sequential palladium and copper catalysis

Trost, Barry M.,Masters, James T.,Taft, Benjamin R.,Lumb, Jean-Philip

, p. 6217 - 6231 (2016)

We present a full account detailing the development of a sequential catalysis strategy for the synthesis of chiral β-alkynyl carbonyl and sulfonyl derivatives. A palladium-catalyzed cross coupling of terminal alkyne donors with acetylenic ester, ketone, a

A new strategy for the synthesis of chiral β-alkynyl esters via sequential palladium and copper catalysis

Trost, Barry M.,Taft, Benjamin R.,Masters, James T.,Lumb, Jean-Philip

supporting information; experimental part, p. 8502 - 8505 (2011/07/08)

A new strategy for the synthesis of chiral β-alkynyl esters which relies on sequential Pd and Cu catalysis is reported. Terminal alkynes bearing aryl, alkyl, and silyl groups can be employed without prior activation yielding a wide range of important chiral building blocks. The reaction sequence utilizes a robust Pd(II)-catalyzed hydroalkynylation of ynoates with terminal alkynes providing geometrically pure ynenoates which are readily reduced by CuH. In contrast to previous reports, where additions to ynenoates proceed with marginal preference for the 1,6-pathway, this conjugate reduction occurs with high 1,4-selectivity yielding β-alkynyl esters with excellent levels of enantioselectivity. Importantly, the method tolerates a wide range of functionality, including allylic carbonates and carbamates, and thus allows for rapid elaboration of the β-alkynyl esters into a variety of chiral, substituted heterocycles.

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