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Results 1 to 25 of 1927

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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

Removal of methoxyethoxymethyl ethers with trimethylsilyl chloride-sodium iodideRIGBY, J. H; WILSON, J. Z.Tetrahedron letters. 1984, Vol 25, Num 14, pp 1429-1432, issn 0040-4039Article

Mild, selective deprotection of PMB ethers with triflic acid/1,3-dimethoxybenzeneJUNG, Michael E; KOCH, Pierre.Tetrahedron letters. 2011, Vol 52, Num 46, issn 0040-4039, 6039, 6051-6054 [5 p.]Article

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 oligodeoxyribonucleotides involving a rapid procedure for removal of base-protecting groups by use of the 4,4',4″-tris(benzoyloxy)trityl (TBTr) groupSEKINE, M; MASUDA, N; HATA, T et al.Bulletin of the Chemical Society of Japan. 1986, Vol 59, Num 6, pp 1781-1789, issn 0009-2673Article

In search of new methods in peptide synthesis. A review of the last three decadesBODANSZKY, M.International journal of peptide & protein research. 1985, Vol 25, Num 5, pp 449-474, issn 0367-8377Article

STUDIES ON PEPTIDES. LXXVI. SYNTHESIS OF KASSININ, A NEW FROG SKIN PEPTIDE.YAJIMA H; SASAKI T; OGAWA H et al.1978; CHEM. PHARM. BULL.; JAP.; DA. 1978; VOL. 26; NO 4; PP. 1231-1235; BIBL. 19 REF.Article

New oxidatively removable carboxy protecting groupsKIM, C. U; MISCO, P. F.Tetrahedron letters. 1985, Vol 26, Num 17, pp 2027-2030, issn 0040-4039Article

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

Solid-supported synthesis, deprotection and enzymatic purification of oligodeoxyribonucleotidesURDEA, M. S; HORN, T.Tetrahedron letters. 1986, Vol 27, Num 26, pp 2933-2936, issn 0040-4039Article

PEPTIDSYNTHESEN MIT 3'-IOD-L-TYROSIN. I: SYNTHESE VON PEPTIDEN MIT O4'-BENZYL-3'-IOD-L-TYROSIN = SYNTHESES DE PEPTIDES CONTENANT L'IODO-3' L-TYROSINE. I: SYNTHESE DE PEPTIDES DE L'O-BENZYL-4' IODO-3' L-TYROSINETARNAWSKI J; RZESZOTARSKA B; NADOLSKA B et al.1979; ANN. (JUSTUS LIEBIGS) CHEM.; DEU; DA. 1979; NO 6; PP. 761-768; ABS. ENG; BIBL. 16 REF.Article

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

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

AN ADVANTAGEOUS METHOD FOR THE RAPID REMOVAL OF HYDROGENOLYSABLE PROTECTING GROUPS UNDER AMBIENT CONDITIONS; SYNTHESIS OF LEUCINE-ENKEPHALINANWER MK; SPATOLA AF.1980; SYNTHESIS (STUTTG.); ISSN 0039-7881; DEU; DA. 1980; NO 11; PP. 929-932; BIBL. 20 REF.Article

ISONICOTINYLOXYCARBONYL, A NOVEL AMINO PROTECTING GROUP FOR PEPTIDE SYNTHESIS.VEBER DF; PALEVEDA WJ JR; LEE YC et al.1977; J. ORG. CHEM.; U.S.A.; DA. 1977; VOL. 42; NO 20; PP. 3286-3288; BIBL. 19 REF.Article

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

Deoximation of oxime O-acetates, oximes, and oxime ethers by nonacarbonyldiiron or pentacarbonyliron: an electronic effect for the N-O bond cleavageNITTA, M; SASAKI, I; MIYANO, H et al.Bulletin of the Chemical Society of Japan. 1984, Vol 57, Num 11, pp 3357-3358, issn 0009-2673Article

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