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Results 1 to 25 of 1392

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Efficient N-p-methoxyphenyl amine deprotection through anodic oxidationDE LAMO MARIA, Sandra; MARTENS, Thierry; MIOSKOWSKI, Charles et al.Journal of organic chemistry. 2005, Vol 70, Num 25, pp 10592-10595, issn 0022-3263, 4 p.Article

3-Methoxybenzyl (3-MPM) and 3,5-dimethoxybenzyl (3,5-DMPM) protecting groups for the hydroxy function less readily removable than 4-methoxybenzyl (MPM) and 3,4-dimethoxybenzyl (DMPM) protecting groups by DDQ oxidationNAKAJIMA, N; ABE, R; YONEMITSU, O et al.Chemical and pharmaceutical bulletin. 1988, Vol 36, Num 10, pp 4244-4247, issn 0009-2363Article

Silver trifluoromethanesulphonate as an S-deprotecting reagent for the synthesis of cystine peptidesFUJII, N; OTAKA, A; WATANABE, T et al.Journal of the Chemical Society. Chemical communications. 1989, Num 5, pp 283-284, issn 0022-4936, 2 p.Article

SYnthesis of 5-homologus AZT and D4T derivativesKJÆRSGAARD, U; PEDERSEN, E. B; NIELSEN, C et al.Acta chemica scandinavica (Copenhagen. 1989). 1992, Vol 46, Num 10, pp 1016-1020, issn 0904-213XArticle

C-nucleosides. XVI : A synthesis of a 1,5-benzodiazepin-2-one homo-C-nucleoside through condensation of 1,2-diaminobenzene with 5-hydroxy-5-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)furan-2(5H)#75oneITO, Y; ITO, C; MAEBA, I et al.Heterocycles (Sendai). 1991, Vol 32, Num 10, pp 1955-1960, issn 0385-5414Article

Selective deprotection of trialkylsilyl etherns using fluorosilicic acidPILCHER, A. S; HILL, D. K; SHIMSHOCK, S. J et al.Journal of organic chemistry. 1992, Vol 57, Num 8, pp 2492-2495, issn 0022-3263Article

Synthesis of 2'-C-cyano-2'-deoxy- and 2'-C-cyano-2',3'-dideoxy-β-D-arabinofuranosyl nucleosidesVELAZQUEZ, S; CAMRASA, M.-J.Tetrahedron (Oxford. Print). 1992, Vol 48, Num 9, pp 1683-1694, issn 0040-4020Article

Syntheses of pyrrolo[2,3d]pyrimidine 2',3'-dideoxyguanosine and inhibitory activity of 5'-triphosphates on HIV-1 reverse transcriptaseSEELA, F; MUTH, H.-P; ROLING, A et al.Helvetica chimica acta. 1991, Vol 74, Num 3, pp 554-564, issn 0018-019XArticle

A new entry for the deprotection of monothioacetals and dithioacetals : silver nitrite : iodine systemNISHIDE, K; YOKOTA, K; NAKAMURA, D et al.Tetrahedron letters. 1993, Vol 34, Num 21, pp 3425-3428, issn 0040-4039Article

Piperidine is preferable to morpholine for Fmoc cleavage in solid phase synthesis of O-linked glycopeptidesKIHLBERG, J; VULJANIC, T.Tetrahedron letters. 1993, Vol 34, Num 38, issn 0040-4039, 5981, 6135-6138 [5 p.]Article

A synthetic procedure for the preparation of oligonucleotides without using ammonia and its application for the synthesis of oligonucleotides containing O-4-alkyl thymidinesERITJA, R; ROBLES, J; AVINO, A et al.Tetrahedron (Oxford. Print). 1992, Vol 48, Num 20, pp 4171-4182, issn 0040-4020Article

Simultaneous synthesis of degenerate oligo-nucleotides of variable lengthJERALA, R.BioTechniques. 1992, Vol 13, Num 4, pp 564-567, issn 0736-6205, 3 p.Article

Resin effect in solid-phase peptide synthesis. Enhanced purity of tryotophan-containing peptides through two-step cleavage of side chain protecting groups and peptide-resin linkageJOHNSON, T; SHEPPARD, R. C.Journal of the Chemical Society. Chemical communications. 1991, Num 22, pp 1653-1655, issn 0022-4936Article

Conversion of N-terminal cysteine to thiazolidine carboxylic acid during hydrogen fluoride deprotection of peptides containing Nπ-bom protected histidineGESQUIERE, J.-C; DIESIS, E; TARTAR, A et al.Journal of the Chemical Society. Chemical communications. 1990, Num 20, pp 1402-1403, issn 0022-4936, 2 p.Article

Susceptibility of glycans to β-elimination in Fmoc-based O-glycopeptide synthesisMELDAL, M; BIELFELDT, T; PETERS, S et al.International journal of peptide & protein research. 1994, Vol 43, Num 6, pp 529-536, issn 0367-8377Article

Cleavage and deprotection of peptides on MBHA-resin with hydrogen bromideWANG, S. S; WANG, B. S. H; HUGHES, J. L et al.International journal of peptide & protein research. 1992, Vol 40, Num 3-4, pp 344-349, issn 0367-8377Article

Highly efficient deprotection of Aromatic acetals under neutral conditions using β-cyclodextrin in watersSRILAKSHMI KRISHNAVENI, N; SURENDRA, K; ARJUN REDDY, M et al.Journal of organic chemistry. 2003, Vol 68, Num 5, pp 2018-2019, issn 0022-3263, 2 p.Article

A total synthesis of hematoside, α-NeuGc-(2→3)β-gal-(1→4)-β-Glc-(1→1)-CerNUMATA, M; SUGIMOTO, M; SHIBAYAMA, S et al.Carbohydrate research. 1988, Vol 174, pp 73-85, issn 0008-6215Article

Rapid deprotection for unpurified synthetic oligonucleotide primers used in DNA sequencingURDEA, M. S; SANCHEZ-PESCADOR, R.BioTechniques. 1987, Vol 5, Num 2, pp 106-110, issn 0736-6205, 2 p.Article

Trimethylsilyl trifluoromethanesulphonate as a useful deprotecting reagent in both solution and solid phase peptide synthesesFUJII, N; OTAKA, A; IKEMURA, O et al.Journal of the Chemical Society. Chemical communications. 1987, Num 4, pp 274-275, issn 0022-4936Article

Post-exposure-bake simulation model with constant acid loss of chemically amplified resistYANAGISHITA, Y; MIYATA, S; KAIMOTO, Y et al.Japanese journal of applied physics. 1997, Vol 36, Num 12B, pp 7611-7614, issn 0021-4922, 1Conference Paper

On the rapid deprotection of synthetic oligonucleotides and analogsPOLUSHIN, N. N; MOROCHO, A. M; BAN-CHIN CHEN et al.Nucleic acids research. 1994, Vol 22, Num 4, pp 639-645, issn 0305-1048Article

Photochemicl reactions of methanesulfonates. A new deprotection reactionBINKLEY, R. W; XIAOGAO LIU.Journal of carbohydrate chemistry. 1992, Vol 11, Num 2, pp 183-188, issn 0732-8303Article

Rapid deprotection of synthetic oligonucleotidesREYNOLDS, T. R; BUCK, G. A.BioTechniques. 1992, Vol 12, Num 4, pp 518-521, issn 0736-6205, 3 p.Article

Amino acid structure and difficult sequences in solid phase peptide synthesisBEDFORD, J; HYDE, C; JOHNSON, T et al.International journal of peptide & protein research. 1992, Vol 40, Num 3-4, pp 300-307, issn 0367-8377Article

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