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2. 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]
3. A new reagent for the tert-butyloxycarbonylation of amino acids. Fujino M; Hatanaka C Chem Pharm Bull (Tokyo); 1967 Dec; 15(12):2015-6. PubMed ID: 5590712 [No Abstract] [Full Text] [Related]
4. [tert-Butylation of the tryptophan indole ring during the removal of the tert-butyloxycarbonyl group (author's transl)]. Löw M; Kisfaludy L; Sohár P Hoppe Seylers Z Physiol Chem; 1978 Dec; 359(12):1643-51. PubMed ID: 738698 [TBL] [Abstract][Full Text] [Related]
5. Activation of carboxylic acids by pyrocarbonates. Synthesis of symmetric anhydrides and esters of N-protected amino acids using dialkyl pyrocarbonates as condensing reagents. Pozdnev VF Int J Pept Protein Res; 1992 Nov; 40(5):407-14. PubMed ID: 1483835 [TBL] [Abstract][Full Text] [Related]
6. [1-Adamanty fluoroformate, a useful reagent in peptide chemistry (author's transl)]. Moroder L; Wackerle L; Wünsch E Hoppe Seylers Z Physiol Chem; 1976 Nov; 357(11):1647-50. PubMed ID: 1002131 [TBL] [Abstract][Full Text] [Related]
7. Tert-butyl fluoroformate, a new reagent for peptide syntheses. Schnabel E; Herzog H; Hoffmann P; Klauke E; Ugi I Angew Chem Int Ed Engl; 1968 May; 7(5):380. PubMed ID: 4968102 [No Abstract] [Full Text] [Related]
8. Transformations of penicillin. II. NN'-di-isopropylhydrazine, a new reagent for protection of carboxylic acids. Barton DH; Girijavallabhan M; Sammes PG J Chem Soc Perkin 1; 1972; 7():929-32. PubMed ID: 5064242 [No Abstract] [Full Text] [Related]
9. [Research on ortho-diacetylbenzene, a reagent for amino groups. I. Study of the reaction with amino acids]. Bourhis M; Jensen H; Neuzil E Ann Pharm Fr; 1970; 28(9):561-74. PubMed ID: 5515400 [No Abstract] [Full Text] [Related]
10. Ruthenium-catalyzed double-fold C-H tertiary alkoxycarbonylation of arenes using di-tert-butyl dicarbonate. Hong X; Wang H; Liu B; Xu B Chem Commun (Camb); 2014 Nov; 50(91):14129-32. PubMed ID: 25275272 [TBL] [Abstract][Full Text] [Related]
11. Convenient and Simple Esterification in Continuous-Flow Systems using g-DMAP. Okuno Y; Isomura S; Sugamata A; Tamahori K; Fukuhara A; Kashiwagi M; Kitagawa Y; Kasai E; Takeda K ChemSusChem; 2015 Nov; 8(21):3587-9. PubMed ID: 26423212 [TBL] [Abstract][Full Text] [Related]
12. [Tests of applying phenyl izoselenocyanate for unveiling N-terminal amino acids of peptides chains and the synthesis of analogoues selenium of PTH-amino acids (author's transl)]. Iskierko J; Klimek J; Górski A; Urban T; Sienkiewicz E Ann Univ Mariae Curie Sklodowska Med; 1976; 31():69-76. PubMed ID: 1032806 [No Abstract] [Full Text] [Related]
13. 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]
14. Curtius rearrangement of aromatic carboxylic acids to access protected anilines and aromatic ureas. Lebel H; Leogane O Org Lett; 2006 Dec; 8(25):5717-20. PubMed ID: 17134255 [TBL] [Abstract][Full Text] [Related]
18. [20,21-aziridine steroids: reaction of derivatives of the oximes of 5-pregnen-20-one, 9beta,10alpha-5-pregnen-20 and 9beta,10alpha-5,7-pregnadiene-20-one with lithium aluminium hydride, and of 3beta-hydroxy-5-pregnen-20-one oxime with Grignard reagents (author's transl)]. Tzikas A; Tamm C; Boller A; Fürst A Helv Chim Acta; 1976 Jun; 59(5):1850. PubMed ID: 931756 [No Abstract] [Full Text] [Related]
19. [NMR study of aqueous solutions of amino acids and nucleotides using a lanthanide shift reagent]. Buikliskiĭ VD; Zolin VF; Koreneva LG; Sheveleva IS; Paniushkin VT Biofizika; 1981; 26(4):615-20. PubMed ID: 7284450 [No Abstract] [Full Text] [Related]
20. N-acylation during the addition of carboxylic acids to N-tert-Butylacylketenimines and the use of the reagent N-tert-Butyl-5-methylisoxazolium Perchlorate for Peptide Synthesis. Woodman DJ; Davidson AI J Org Chem; 1973 Dec; 38(25):4288-95. PubMed ID: 4778124 [No Abstract] [Full Text] [Related] [Next] [New Search]