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tert-butyl (2R)-2-{(1R,2S)-2-methoxy-2-methyl-1-[(triphenylmethylsulfenyl)amino]pentyl}-5-oxo-2,5-dihydro-1H-pyrrole-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

335693-23-7

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335693-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 335693-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,6,9 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 335693-23:
(8*3)+(7*3)+(6*5)+(5*6)+(4*9)+(3*3)+(2*2)+(1*3)=157
157 % 10 = 7
So 335693-23-7 is a valid CAS Registry Number.

335693-23-7Relevant academic research and scientific papers

A highly diastereoselective vinylogous Mannich condensation and 1,4-conjugate addition of (Z)-propenyl cuprate in the synthesis of an influenza neuraminidase inhibitor

Barnes, David M.,Bhagavatula, Lakshmi,DeMattei, John,Gupta, Ashok,Hill, David R.,Manna, Sukumar,McLaughlin, Maureen A.,Nichols, Paul,Premchandran, Ramiya,Rasmussen, Michael W.,Tian, Zhenping,Wittenberger, Steven J.

, p. 3541 - 3551 (2007/10/03)

A practical synthesis of neuraminidase influenza inhibitor, A-322278, has been developed. Asymmetry is introduced into the synthesis by an enzyme mediated ester hydrolysis. A highly diastereoselective vinylogous Mannich condensation reaction of N-Boc-2-te

Enantioselective synthesis of antiinfluenza compound A-315675

DeGoey, David A.,Chen, Hui-Ju,Flosi, William J.,Grampovnik, David J.,Yeung, Clinton M.,Klein, Larry L.,Kempf, Dale J.

, p. 5445 - 5453 (2007/10/03)

Drug discovery efforts at Abbott Laboratories have led to the identification of influenza neuraminidase inhibitor A-315675 (1) as a candidate for development as an antiinfluenza drug. A convergent, stereoselective synthesis of this highly functionalized pyrrolidine is reported that utilizes pyrrolinone 2 as the key intermediate. The C5, C6 stereochemistry was established through a diastereoselective condensation of chiral imine compound 3 with silyloxypyrrole 4 to give pyrrolinone 2. The stereochemical outcome of this reaction depended critically on the choice of the imine functional group (FG), with tritylsulfenyl and (R)-toluenesulfinyl providing the desired products in good yields as crystalline intermediates. Conversion of pyrrolinone 2 into 1 was accomplished in seven subsequent steps, including Michael addition of cis-1-propenylcuprate at C4 and introduction of a cyano group as a carboxylic acid equivalent at C2.

Synthesis of an influenza neuraminidase inhibitor intermediate via a highly diastereoselective coupling reaction.

Barnes, David M,McLaughlin, Maureen A,Oie, Tetsuro,Rasmussen, Michael W,Stewart, Kent D,Wittenberger, Steven J

, p. 1427 - 1430 (2007/10/03)

[reaction: see text]. A highly diastereoselective coupling reaction between TBSOP (3) and trityl sulfenimine 4 was developed which provided influenza neuraminidase inhibitor intermediate 7 in 80% yield and >99% de after crystallization. The reaction was shown to be reversible with the high diastereoselectivity resulting from a favorable H-bonding interaction in the major diastereomer.

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