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Showing 1 to 20 of 136 for “"deprotection"”.

  1. Control of regioselectivity:oxidation and deprotection

    … over a palladium catalyst. Oxidative deprotection methods are also available, particularly when the MPM (4-methoxybenzyl) group is used in place of Bn. The NAP (2-naphthylmethyl) protective group has recently been introduced and has been shown to be removed by hydrogenolysis more …

    cambridge Repository record for Control of regioselectivity:oxidation and deprotection (opens in a new tab)

  2. Synthesis and Application of Boronic Acid Derivatives

    … During the synthesis of this compound, published deprotection methods were not suitable to deprotect the pinacol group. A two-step protocol for pinacolyl boronic ester deprotection via a diethanolamine protected intermediate was successfully developed with the advantages of mild reaction …

    vt Repository record for Synthesis and Application of Boronic Acid Derivatives (opens in a new tab)

  3. Total Synthesis and Stereochemical Revision of Pestalospirane B

    … natural product. Initial attempts at late stage deprotection of isopropyl dimer 314 were unsucessful, thus a revision in protecting group strategy was enforced where access to the natural product was envisioned to allow deprotection prior to dimerisation of acetal 342. Attention, therefore …

    auckland-ms Repository record for Total Synthesis and Stereochemical Revision of Pestalospirane B (opens in a new tab)

  4. Synthesis and Antifungal Evaluation of Barbiturate Saponins And Progress Towards Cysteinyl Metal Peptides

    … the barbiturate without requiring protection and deprotection of saccharides. Efficient methods were developed for synthesis of 3<em>β</em> derivatized steroid derivatives containing ether, carbonate, ester and carbamate linker. Synthesized mono and disaccharide barbiturates were incorporated into …

    uno Repository record for Synthesis and Antifungal Evaluation of Barbiturate Saponins And Progress Towards Cysteinyl Metal Peptides (opens in a new tab)

  5. Preparation of arylphosphinic acid derivatives as building blocks for binding sites

    … derived from methyl phosphinate. Deprotection of the bisphenylalanylphosphinate and mixing it with a metal ion lead to self-assembled cyclic metal complex of bisphenylalanyl phosphinic acid. Selective deprotection and peptide coupling of bisphenylalanylphosphinate generate a …

    iastate Repository record for Preparation of arylphosphinic acid derivatives as building blocks for binding sites (opens in a new tab)

  6. Synthesis of Delta(3)-Imidazolines as Latent Forms of Peptidyl Trifluoromethyl Ketones

    … ketones during typical peptide Fmoc deprotection and elongation reactions. In the final step, the imidazoline was hydrolyzed with dilute acid, which afforded the trifluoromethyl ketone in good yield. This process was carried out without the use of oxidants and was shown not to affect …

    uiuc Repository record for Synthesis of Delta(3)-Imidazolines as Latent Forms of Peptidyl Trifluoromethyl Ketones (opens in a new tab)

  7. Telomere-Driven Tetraploidy and its Relevance to Cancer

    … in early tumorigene sis. Prolonged telomere deprotection caused by inactivation of the telomeric proteins POT1a and POT1b leads to tetraploidy in p53/Rb de cient mouse cells. Irreversible telomere deprotection and other forms of persistent DNA damage induce a prolonged G2 phase followed by …

    rockefeller Repository record for Telomere-Driven Tetraploidy and its Relevance to Cancer (opens in a new tab)

  8. The use of immobilised crown ethers as in-situ protecting groups for organic synthesis within flow reactors

    … pathway (by at least two steps – protection and deprotection), generally leading to an increase in cost and a decrease in yield. The protecting group is often selected based upon the deprotection conditions, leading to the requirement for orthogonal protecting groups. Crown ethers are commonly …

    hull Repository record for The use of immobilised crown ethers as in-situ protecting groups for organic synthesis within flow reactors (opens in a new tab)

  9. A small molecule synthesizer

    … and are universally susceptible to general mild deprotection conditions. Additionally, MIDA boronates can be prepared by a variety of synthetic methods on multi-gram scale and they demonstrate significantly improved reaction yields with slow-addition cross-coupling (SACC). It was understood that …

    uiuc Repository record for A small molecule synthesizer (opens in a new tab)

  10. Living Polymerization for the Introduction of Tailored Hydrogen Bonding

    … initiated polyisoprenes proved that facile deprotection was not possible and residual catalyst was not removable from the polymer. However, polymers initiated with 3-(t-butyldimethylsilyloxy)-1-propyllithium were quantitatively hydrogenated and deprotected under relatively mild conditions to …

    vt Repository record for Living Polymerization for the Introduction of Tailored Hydrogen Bonding (opens in a new tab)

  11. Solid Phase Synthesis of M-Phenylene Ethynylene Oligomer Heterosequences

    … days, efforts were taken to limit the need for deprotection steps and ensure cross-coupling conditions were complete within two hours. This led to the ability to produce mPE heterosequence hexamers with aryl bromide and terminal acetylene endgroups in good yields (typically 55-75%), in twelve …

    uiuc Repository record for Solid Phase Synthesis of M-Phenylene Ethynylene Oligomer Heterosequences (opens in a new tab)

  12. Synthesis and structure-activity relationships of ring D alkyl 19-norsteroids

    … of which furnished the 16β-alcohol. Routine deprotection of the epimeric pair of methylene 16-alcohols gave the derived estriol analogues, which were subjected to biological evaluation. Treatment of the 14α,15α methylene16-ketone with lithium in liquid ammonia gave …

    cape-town Repository record for Synthesis and structure-activity relationships of ring D alkyl 19-norsteroids (opens in a new tab)

  13. Synthesis of P-Stereogenic Bisphosphine Ligands: Application as Hemi-labile Ligands in the Asymmetric Pauson-Khand Reaction

    … enantiomeric ratio up to 99:1 er. After borane deprotection of the bisphosphines using DABCO, hemi-labile ligands A and B were obtained. These hemi-labile ligands contain a phosphorus lone pair as a strong coordinating group and a sulfur lone pair on the P=S group as a weak coordinating group. …

    whiterose Repository record for Synthesis of P-Stereogenic Bisphosphine Ligands: Application as Hemi-labile Ligands in the Asymmetric Pauson-Khand Reaction (opens in a new tab)

  14. Synthesis of triplex-forming oligonucleotide conjugates of the anticancer drug temodal

    … were evaluated. A novel cleavage and deprotection procedure was developed which allowed for the solid phase synthesis of the base-sensitive TFO-drug conjugates using a recently developed silyl-linked controlled pore glass (SLCPG) support. Covalent attachment of either temozolomide or …

    aston Repository record for Synthesis of triplex-forming oligonucleotide conjugates of the anticancer drug temodal (opens in a new tab)

  15. Synthesis and structure-activity studies of skeletally modified estradiol analogues

    … 17β-diol, by a hydrogenation, desulfonylation, deprotection reaction sequence. The unexpectedly complex result for the cycloaddition reaction was interpreted with the assistance of other cycloaddition reactions of the Δ¹⁴,¹⁶-dienyl acetate. 17,17-Ethylenedioxy-3-methoxy-9β-estra-l …

    cape-town Repository record for Synthesis and structure-activity studies of skeletally modified estradiol analogues (opens in a new tab)

  16. Synthesis of aza-tryptophan derivatives.

    … intended product. Subsequent deoxygenation and deprotection of the indole, ring, and the amino and acid functional groups yielded racemic 7-azatryptophan A variety of attempts to synthesize the enantiomerically pure form of 7-azatryptophan were considered. Of those Evans' asymmetric glycine …

    windsor Repository record for Synthesis of aza-tryptophan derivatives. (opens in a new tab)

  17. Chemical synthesis of glycosylated oligoribonucleotides for siRNA development

    … were synthesized from perbenzylated ribolactone. Deprotection of benzyl-protected ribofuranosyl phenanthrene and pyrene by boron tribromide gave ribofuranosyl phenanthrene and ribopyranosyl pyrene, respectively. UV/vis and fluorescent properties of the ribosides were characterized.

    brock Repository record for Chemical synthesis of glycosylated oligoribonucleotides for siRNA development (opens in a new tab)

  18. Synthetic studies on Canangone and beta-Chamigrene

    … hydrolysis provided the spirolactone. Subsequent deprotection, Luche reduction and oxidation gave (R*,R*) Canangone and (5R*,6S*)-epi-Canangone. Following the same strategy, optically active (+)-Canangone and (-)-Canangone, and their epimers were synthesized. As a second target, the synthesis of …

    oldenburg Repository record for Synthetic studies on Canangone and beta-Chamigrene (opens in a new tab)

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