The synthesis of oligoribonucleotides. III. The use of silyl protecting groups in nucleoside and nucleotide chemistry. VIII

1979 ◽  
Vol 57 (17) ◽  
pp. 2230-2238 ◽  
Author(s):  
Kelvin K. Ogilvie ◽  
Aria L. Schifman ◽  
Christopher L. Penney

The synthesis of all isomeric mono- and disilyl derivatives of cytidine, guanosine, and their N-benzoyl analogues using the tert-butyldimethylsilyl protecting group is described. These compounds and those containing a 5′-monomethoxytrityl group have been condensed via the phosphodichloridite procedure to produce nucleotides rapidly and in good yields. The synthesis of 2′–5′-linked nucleotides is described. A cautionary note is introduced in regard to the preparation of 5′-monomethoxytritylguanosine and a novel methanolysis of certain N-benzoylcytidines is mentioned.

2021 ◽  
Author(s):  
◽  
Thomas Bevan

<p>Azulene is a hydrocarbon that exhibits an intense blue colour. Derivatives of azulene exhibit different colours depending on the position and electronic properties of the substituents. The chemical and chromophoric properties of azulene and guaiazulene derivatives are investigated for the potential use in applications such as chromophoric protecting groups and self-indicating scavenger resins. Investigations were carried out on the scope of known reactions on the 3- position of guaiazulene for this purpose...</p>


2021 ◽  
Author(s):  
◽  
Thomas Bevan

<p>Azulene is a hydrocarbon that exhibits an intense blue colour. Derivatives of azulene exhibit different colours depending on the position and electronic properties of the substituents. The chemical and chromophoric properties of azulene and guaiazulene derivatives are investigated for the potential use in applications such as chromophoric protecting groups and self-indicating scavenger resins. Investigations were carried out on the scope of known reactions on the 3- position of guaiazulene for this purpose...</p>


2005 ◽  
Vol 70 (12) ◽  
pp. 2075-2085 ◽  
Author(s):  
Jiří Kroutil ◽  
Klára Jeništová

Aziridine ring cleavage reactions of five N-nosylepimines (2-6) having D-talo, D-galacto, D-manno, and D-allo configurations with potassium hydrogendifluoride under various reaction conditions have been performed. The cleavage regioselectively afforded diaxial isomers of vicinal amino-fluoro derivatives of 1,6-anhydro-β-D-gluco- and mannopyranose 7-11 in 51-94% yields. Removal of 2-nitrobenzenesulfonyl protecting group with benzenethiol has been attempted in the case of compound 10.


Biomedicines ◽  
2021 ◽  
Vol 9 (6) ◽  
pp. 678
Author(s):  
Carlo Diaferia ◽  
Elisabetta Rosa ◽  
Enrico Gallo ◽  
Giovanni Smaldone ◽  
Mariano Stornaiuolo ◽  
...  

Peptide-based hydrogels (PHGs) are biocompatible materials suitable for biological, biomedical, and biotechnological applications, such as drug delivery and diagnostic tools for imaging. Recently, a novel class of synthetic hydrogel-forming amphiphilic cationic peptides (referred to as series K), containing an aliphatic region and a Lys residue, was proposed as a scaffold for bioprinting applications. Here, we report the synthesis of six analogues of the series K, in which the acetyl group at the N-terminus is replaced by aromatic portions, such as the Fmoc protecting group or the Fmoc-FF hydrogelator. The tendency of all peptides to self-assemble and to gel in aqueous solution was investigated using a set of biophysical techniques. The structural characterization pointed out that only the Fmoc-derivatives of series K keep their capability to gel. Among them, Fmoc-K3 hydrogel, which is the more rigid one (G’ = 2526 Pa), acts as potential material for tissue engineering, fully supporting cell adhesion, survival, and duplication. These results describe a gelification process, allowed only by the correct balancing among aggregation forces within the peptide sequences (e.g., van der Waals, hydrogen bonding, and π–π stacking).


2006 ◽  
Vol 84 (10) ◽  
pp. 1250-1253 ◽  
Author(s):  
Mee-Kyung Chung ◽  
Paul Fancy ◽  
Jeffrey M Stryker

The direct synthesis of sterically hindered, partially etherified derivatives of tetrakis(2-hydroxyphenyl)ethene is reported by using the McMurry reductive olefination reaction on a range of differentially substituted 2,2′-dialkoxy benzophenone substrates. Three orthogonal protection strategies are demonstrated, incorporating β-silylethyl, 3-butenyl, and tert-butyl protecting groups, respectively, into the starting benzophenones. The latter proved most efficient, with both the McMurry coupling and deprotection steps occurring concomitantly under the McMurry conditions to directly yield the desired bis(2-hydroxyphenyl)-bis(2-methoxyphenyl)ethene as a 1:1 mixture of E- and Z-diastereoisomers.Key words: preorganized polyaryloxide ligands, McMurry olefination, titanium trichloride, supramolecular chemistry, tetrakis(2-hydroxyphenyl)ethene, 2,2′-disubstituted benzophenone.


Author(s):  
Jie Jack Li ◽  
Chris Limberakis ◽  
Derek A. Pflum

In his book, Protecting Groups, Philip J. Kocieński stated that there are three things that cannot be avoided: death, taxes, and protecting groups. Indeed, protecting groups mask functionality that would otherwise be compromised or interfere with a given reaction, making them a necessity in organic synthesis. In this chapter, for each protecting group showcased, only the most widely used methods for protection and cleavage are shown. Also, this section is not comprehensive and only addresses some of the most common blocking groups in organic synthesis. For a thorough review of protecting groups, the reader should consult the following references: (a) Wuts, P. G. M.; Greene, T. W.; Protective Groups in Organic Synthesis, 4th ed.; Wiley: Hoboken, NJ, 2007; (b) Kocienski, P. J. Protecting Groups, 3rd edition.; Thieme: Stuggart, 2004. In this section, the formation and cleavage of eight protecting groups for alcohols and phenols are presented: acetate; acetonides for diols; benzyl ether; para-methoxybenzyl (PMB) ether; methyl ether; methoxymethylene (MOM) ether; tert-butyldiphenylsilyl (TBDPS) silyl ether; and tetrahydropyran (THP). Acetate is a convenient protecting group for alcohols—easy on and easy off. Selective protection of a primary alcohol in the presence of a secondary alcohol can be achieved at low temperature. The drawback of this protecting group is its incompatibility with hydrolysis and reductive conditions.


1982 ◽  
Vol 35 (4) ◽  
pp. 795 ◽  
Author(s):  
W Cowden ◽  
NW Jacobsen

5-Ethyl-1,3-dihydroxy-5-phenylbarbituric acid (N,N'-dihydroxyphenobarbital) and 5,5-diethyl-1,3-dihydroxybarbituric acid (N,N'-dihydroxyveronal) have been prepared by the condensation of 1,3-dibenzyloxyurea with ethylphenylmalonyl dichloride and diethylmalonyl dichloride respectively, followed by the removal of the benzyl protecting groups from the intermediate dibenzyloxy derivatives.


1969 ◽  
Vol 22 (11) ◽  
pp. 2451 ◽  
Author(s):  
FHC Stewart

Various esters and salts of N-nitrososarcosine and N-nitroso-L-proline have been prepared, and used to provide amino and carboxyl components in model peptide syntheses. The sequential polypeptide (Sar-Gly)n was synthesized using the nitroso residue as an acid-sensitive protecting group. ��� Anomalous behaviour of some of the N-nitroso derivatives in the Liebermann colour reaction is also discussed.


2017 ◽  
Vol 19 (9) ◽  
pp. 2140-2144 ◽  
Author(s):  
Hong-Shuang Wang ◽  
Hui-Jing Li ◽  
Jun-Li Wang ◽  
Yan-Chao Wu

The atom- and step-economical synthesis of seven puupehenone- and haterumadienone-type marine natural products without the use of protecting groups and transition metals has been achieved from the abundant feedstock chemical sclareolide in only 6 to 9 steps.


Synthesis ◽  
2017 ◽  
Vol 50 (05) ◽  
pp. 1113-1122 ◽  
Author(s):  
Santosh Tilve ◽  
Sandesh Bugde ◽  
Prajesh S.Volvoikar

An efficient synthesis of naturally occurring 1,2- and 1,3-amino alcohol unit containing 2-substituted piperidine alkaloids and their analogues has been developed from l-pipecolinic acid. The protocol describes the regio- and stereoselective oxymercuration–demercuration of 2-alkenyl piperidines based on protecting groups to give piperidine alkaloids as a key step.


Sign in / Sign up

Export Citation Format

Share Document