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DOCETAXEL ANHYDROUS

Known as: N-Debenzoyl-N-(tert-butoxycarbonyl)-10-deacetylpaclitaxel, N-Debenzoyl-N-(tert-butoxycarbonyl)-10-deacetyltaxol, N-debenzoyl-N-tert-butoxycarbonyl-10-deacetyltaxol 
The anhydrous form of docetaxel, a semisynthetic side-chain analogue of paclitaxel with antineoplastic property. Docetaxel binds specifically to the… Expand
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
A high-throughput screen of the NIH molecular libraries sample collection and subsequent optimization of a lead dipeptide-like… Expand
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Highly Cited
2012
Highly Cited
2012
A simple, environmentally friendly, and very efficient procedure for the synthesis of optically pure N-(tert-butylsulfinyl)imines… Expand
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Highly Cited
2007
Highly Cited
2007
The feasibility of stir-bar sorptive extraction (SBSE) followed by liquid desorption in combination with large volume injection… Expand
Highly Cited
2007
Highly Cited
2007
As the most electronegative element, fluorine has attracted enormous attention recently in the fields of agricultural and… Expand
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Highly Cited
2006
Highly Cited
2006
This paper reports an improved silylation procedure for simultaneous determination of the steroid hormones 17alpha… Expand
Highly Cited
2005
Highly Cited
2005
We describe an enantioselective synthetic route to the antiproliferative alkaloid stephacidin B (1) proceeding in 18 steps and 4… Expand
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Highly Cited
2001
Highly Cited
2001
A very general reaction is presented to achieve the nucleophilic transfer of "CF3 " to chiral N-(tert-butylsulfinyl)imines in… Expand
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Highly Cited
1997
Highly Cited
1997
Asymmetric hydroformylation of heterocyclic olefins catalyzed by phosphine-phosphite-Rh(I) complexes has been investigated… Expand
Highly Cited
1992
Highly Cited
1992
A convenient synthesis of 4-nitrobenzyl-substituted macrocyclic tetraamines and their conversion to bifunctional poly(amino… Expand
Highly Cited
1991
Highly Cited
1991
A variety of synthetic analogues of taxol, a naturally occurring antitumor diterpene, were examined for their potency to inhibit… Expand