Sentence examples for protected 1 from inspiring English sources

That need also vindicated concepts such as the ARG and the spearhead battalion (the capacity in which 1 PARA was serving when it deployed), and protected 1 PARA in the 2004 review of the infantry structure.

An obvious idea is that, if normal cells could be reversibly prevented from dividing during the time of chemotherapy, they would be protected 1.

The P38 kinase inhibitor SB202190 protected 1 mM SNP-mediated chondrocyte death only at 10 μM, which may inhibit pathways other than p38 (Fig. 5b).

In the last step, the tert-butoxycabonyl (Boc) protected 1 required particularly mild deprotection with 70%% formic acid, as other standard conditions resulted in cleavage of the side-chain cylcooctyne moiety.

Internal alkynes 446 tethered to a furan through a protected benzylic alcohol react with gold(I) giving protected 1-naphthol derivatives 448 via formation of a cationic intermediate 447, followed by ring-opening of the furan ring and aromatization (Scheme 146).

"High-ranking prelates protected 58 colleagues from disgrace rather than protecting children from these predator priests".

A straightforward route for preparing orthogonally protected 1,2,4-oxadiazole-bearing dipeptide building blocks is presented.

The rationally designed lactosamine-3,2′-diol derivative with an orthogonal set of protecting groups is efficiently glycosylated with a benzyl protected 1-thio-l-fucoside donor in a unique regioselective manner to produce Lewis x (Lex) and Lewis y (Ley) derivatives in good yields.

Stereomeric 3-carboxy-Δ2-isoxazoline cyclopentane amino acids, which represent restricted conformations of glutamic acid, have been prepared through a strategy based on the 1,3-carboxy-Δ2-isoxazoline cyclopentaneonylformonitrile 3-carboxy-Δ2-isoxazoline cyclopentane-cyclopent-2-enecarboxylic 3-carboxy-Δ2-isoxazoline cyclopentane

Aza-analogue of the basic disaccharide unit of heparane sulfate was designed as a potent inhibitor against heparanase produced by solid tumors cell, and synthesized via a coupling reaction of phenyl 2-azide-1-thio-d-glucopyranoside derivatives with a partially protected 1-deoxynojirimycin derived from d-glucose.

The edges of platforms must also be protected [5].