175 related articles for article (PubMed ID: 11606219)
1. Fast, efficient and selective deprotection of the tert-butoxycarbonyl (Boc) group using HCl/dioxane (4 m).
Han G; Tamaki M; Hruby VJ
J Pept Res; 2001 Oct; 58(4):338-41. PubMed ID: 11606219
[TBL] [Abstract][Full Text] [Related]
2. Use of 6 M HCl for removal of the N-alpha-tert-butyloxycarbonyl group during solid-phase peptide synthesis.
Naharissoa H; Sarrade V; Follet M; Calas B
Pept Res; 1992; 5(5):293-9. PubMed ID: 1450524
[TBL] [Abstract][Full Text] [Related]
3. Synthesis of peptides using tert-butyloxycarbonyl (Boc) as the α-amino protection group.
Pedersen SW; Armishaw CJ; Strømgaard K
Methods Mol Biol; 2013; 1047():65-80. PubMed ID: 23943478
[TBL] [Abstract][Full Text] [Related]
4. Aqueous phosphoric acid as a mild reagent for deprotection of tert-butyl carbamates, esters, and ethers.
Li B; Berliner M; Buzon R; Chiu CK; Colgan ST; Kaneko T; Keene N; Kissel W; Le T; Leeman KR; Marquez B; Morris R; Newell L; Wunderwald S; Witt M; Weaver J; Zhang Z; Zhang Z
J Org Chem; 2006 Nov; 71(24):9045-50. PubMed ID: 17109528
[TBL] [Abstract][Full Text] [Related]
5. Identification and suppression of decomposition during carbodiimide-mediated reactions of Boc-amino acids with phenols, hydroxylamines and amino acid ester hydrochlorides.
Benoiton NL; Lee YC; Chen FM
Int J Pept Protein Res; 1993 Jun; 41(6):587-94. PubMed ID: 8349416
[TBL] [Abstract][Full Text] [Related]
6. Amino acid deletion products resulting from incomplete deprotection of the Boc group from Npi-benzyloxymethylhistidine residues during solid-phase peptide synthesis.
Yoshizawa-Kumagaye K; Nishiuchi Y; Nishio H; Kimura T
J Pept Sci; 2005 Jul; 11(8):512-5. PubMed ID: 15761875
[TBL] [Abstract][Full Text] [Related]
7. Alcohols and di-tert-butyl dicarbonate: how the nature of the Lewis acid catalyst may address the reaction to the synthesis of tert-butyl ethers.
Bartoli G; Bosco M; Carlone A; Dalpozzo R; Locatelli M; Melchiorre P; Sambri L
J Org Chem; 2006 Dec; 71(26):9580-8. PubMed ID: 17168573
[TBL] [Abstract][Full Text] [Related]
8. Syntheses of 4-[N-(tert-butoxycarbonyl)aminoacyloxymethyl]-3-nitrobenzoic acids for use in the liquid-phase peptide synthesis.
Hemmasi B; Stüber W; Bayer E
Hoppe Seylers Z Physiol Chem; 1982 Jul; 363(7):701-8. PubMed ID: 7129361
[TBL] [Abstract][Full Text] [Related]
9. HF cleavage and deprotection procedures for peptides synthesized using a Boc/Bzl strategy.
Pennington MW
Methods Mol Biol; 1994; 35():41-62. PubMed ID: 7894608
[No Abstract] [Full Text] [Related]
10. Mild and Efficient Preparation of Phytosteryl Amino Acid Ester Hydrochlorides and Their Emulsifying Properties.
Jia C; Xia X; Liu P; Wang H; Zhang J; Zhang X
J Agric Food Chem; 2019 Feb; 67(6):1749-1759. PubMed ID: 30657680
[TBL] [Abstract][Full Text] [Related]
11. Selective tert-butyl ester deprotection in the presence of acid labile protecting groups with use of ZnBr2.
Kaul R; Brouillette Y; Sajjadi Z; Hansford KA; Lubell WD
J Org Chem; 2004 Sep; 69(18):6131-3. PubMed ID: 15373501
[TBL] [Abstract][Full Text] [Related]
12. Comparison of 55% TFA/CH2Cl2 and 100% TFA for Boc group removal during solid-phase peptide synthesis.
Blondelle SE; Houghten RA
Int J Pept Protein Res; 1993 Jun; 41(6):522-7. PubMed ID: 8349409
[TBL] [Abstract][Full Text] [Related]
13. tert.-Butyl aminocarbonate (tert.-butyloxycarbonyloxyamine)--a new acylating reagent for amines.
Harris RB; Wilson IB
Int J Pept Protein Res; 1984 Jan; 23(1):55-60. PubMed ID: 6698715
[TBL] [Abstract][Full Text] [Related]
14. Solid phase peptide synthesis on hydrophilic supports. Part II--Studies using Perloza beaded cellulose.
Englebretsen DR; Harding DR
Int J Pept Protein Res; 1992 Dec; 40(6):487-96. PubMed ID: 1286932
[TBL] [Abstract][Full Text] [Related]
15. Preferred conformation of the tert-butoxycarbonyl-amino group in peptides.
Benedetti E; Pedone C; Toniolo C; Némethy G; Pottle MS; Scheraga HA
Int J Pept Protein Res; 1980 Aug; 16(2):156-72. PubMed ID: 7007264
[TBL] [Abstract][Full Text] [Related]
16. A convergent liquid-phase synthesis of salmon calcitonin.
Lee YS; Lee HJ; Pozdnyakov PI; Samukov VV; Kim HJ
J Pept Res; 1999 Oct; 54(4):328-35. PubMed ID: 10532238
[TBL] [Abstract][Full Text] [Related]
17. Boiling water-catalyzed neutral and selective N-Boc deprotection.
Wang J; Liang YL; Qu J
Chem Commun (Camb); 2009 Sep; (34):5144-6. PubMed ID: 20448974
[TBL] [Abstract][Full Text] [Related]
18. In situ neutralization in Boc-chemistry solid phase peptide synthesis. Rapid, high yield assembly of difficult sequences.
Schnölzer M; Alewood P; Jones A; Alewood D; Kent SB
Int J Pept Protein Res; 1992; 40(3-4):180-93. PubMed ID: 1478777
[TBL] [Abstract][Full Text] [Related]
19. Efficient solid phase peptide synthesis. Use of methanesulfonic acid alpha-amino deprotecting procedure and new coupling reagent, 2-(benzotriazol-1-yl)oxy-1,3-dimethylimidazolidinium hexafluorophosphate (BOI).
Kiso Y; Fujiwara Y; Kimura T; Nishitani A; Akaji K
Int J Pept Protein Res; 1992; 40(3-4):308-14. PubMed ID: 1335997
[TBL] [Abstract][Full Text] [Related]
20. Toward the next-generation drug delivery vehicle: synthesis of a dendrimer with four orthogonally reactive groups.
Lim J; Simanek EE
Mol Pharm; 2005; 2(4):273-7. PubMed ID: 16053330
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]