136693-03-3Relevant academic research and scientific papers
Economical route for oxidative cleavage of double bond to synthesize taxol side chain
Bhatia, Sumati,Singh, Sukhdev,Kumar, Rajesh,Kumar, Amit,Olsen, Carl E.,Prasad, Ashok K.
, p. 379 - 386 (2013/05/08)
An efficient, economical and industry-friendly methodology has been developed for the synthesis of C-13 side chain of taxol, (2R,3S)-3-benzamido-2- hydroxy-3-phenylpropanoic acid by oxidative cleavage of alkene precursor N-[(1S,2S)-2-(1′-ethoxyethoxy)-1-p
PROCESS FOR PREPARING OXAZOLIDINE DERIVATIVES
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Page/Page column 11, (2008/06/13)
A process for preparing (4S,5R)-5-carboxymethyl-2,2-dimethyl-4-phenyl-oxazolidine-3-carboxylic acid t-butyl ester, an intermediate in the preparation of anticancer compounds having a taxane skeleton, such as paclitaxel, docetaxol, etc.
Lipase-Catalyzed Kinetic Resolution of 4-(N-Boc-amino)-1-alken-3-ols
Oshitari, Tetsuta,Mandai, Tadakatsu
, p. 2374 - 2376 (2007/10/03)
A wide range of 4-(N-Boc-amino)-1-alken-3-ols were efficiently resolved by lipase-catalyzed kinetic resolution. This procedure has been successfully applied to the highly enantioselective synthesis of the taxol side chain.
Stereoselective synthesis of L-733,060
Bhaskar,Rao, B. Venkateswara
, p. 915 - 917 (2007/10/03)
Enantioselective synthesis of non-peptidic neurokinin NK1 receptor antagonist L-733,060 is described using ring-closing metathesis as a key step, starting from L-phenylglycine.
Synthetic application of chiral 4-methoxy-2-oxazolidinone synthons to 2-amino alcohols of biological interest
Ishizuka, Tadao,Morooka, Kohei,Ishibuchi, Seigo,Kunieda, Takehisa
, p. 837 - 848 (2007/10/03)
The versatility as chiral synthons of (4S, 5S)- and (4R, 5R)-5-allyl-4-methoxy-2-oxazolidinones, readily obtainable from 3-[(1S)-2-exo-alkoxy-1-apocamphanecarbonyl]-2-oxazolone, is demonstrated by the facile stereospecific conversions to (2R, 3S)-3-amino-2-hydroxy-3-phenylpentanoic acid, (2R, 3R, 5E, 7E)-2-amino-5,7-tetradecadien-3-ol and (2S, 3R)-dihydrosphingosine.
Stereoselective vinylation of amino aldehydes using 2-trimethylsilylethylidentriphenylphosphorane
Franciotti,Mann,Taddei
, p. 6783 - 6786 (2007/10/02)
2-Trimethylsilylethylidentriphenylphosphorane reacts stereoselectively with α-amino aldehydes giving the Cram chelation controlled product of vinylation of the carbonyl group. The olefinic 1,2-amino alcohols obtained with this reaction are important inter
