Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Norbert Rumpf"'
Publikováno v:
Helvetica Chimica Acta. 98:1061-1066
Two different synthetic concepts led to the formation of 17, 19, and 29, the first structural isomeric benzobis[1,3]oxathiins. Hetero-DielsAlder reactions of diethyl mesoxylate 14 and the open valence isomers of the benzobisthietes 12 and 18 yielded
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f29499ed08334a546378604215a3e31
https://doi.org/10.1002/hlca.201500083
https://doi.org/10.1002/hlca.201500083
Autor:
Herbert Meier, Norbert Rumpf
Publikováno v:
Tetrahedron Letters. 39:9639-9642
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce858dae26b2a23a18588cba27b17d55
https://doi.org/10.1016/s0040-4039(98)02265-5
https://doi.org/10.1016/s0040-4039(98)02265-5
Publikováno v:
Journal of Heterocyclic Chemistry. 35:1505-1508
2-(1H-Benzotriazol-1-ylmethyl)-1-naphthalenol (1) can be transformed in high yields to the corresponding thiol 4. Flash vacuum pyrolysis of 4 leads to 2H-naphtho[1,2-b]thiete (5). The benzotriazolyl group proved to be a good leaving group; however, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb8a00d8145be0d4c1f5706c46126070
https://doi.org/10.1002/jhet.5570350648
https://doi.org/10.1002/jhet.5570350648
Publikováno v:
Liebigs Annalen. 1995:2221-2226
Naphtothietes and Their Application to the Synthesis of Heterocycles The three isomeric naphthothietes 5, 11, and 16 were prepared according to the reaction sequences shown in Schemes 1–3. The final step was in each case a flash vacuum pyrolysis (F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bc1a72307dcb89c77688283a427d92f
https://doi.org/10.1002/jlac.1995199512308
https://doi.org/10.1002/jlac.1995199512308
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01b9e431af77a4307aa3b261ac1c8b6b
https://doi.org/10.1002/chin.199918096
https://doi.org/10.1002/chin.199918096
Autor:
Penny Bryant, Sibu Balan, Ji-Won Choi, Manuchehr Porssa, Estera Pawlisz, Steve Brocchini, Yuehua Cong, Ruchi Singh, Norbert Rumpf, Antony Godwin, Keith Powell
Publikováno v:
PEGylated Protein Drugs: Basic Science and Clinical Applications ISBN: 9783764386788
Site-specific PEGylation reagents have been developed that undergo thiol-specific bis-alkylation with the two cysteine sulphur atoms from a native accessible disulphide in proteins. The process for this approach of site-specific PEGylation involves t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e303a8832e7f4dfb89fc517b0474aadd
https://doi.org/10.1007/978-3-7643-8679-5_4
https://doi.org/10.1007/978-3-7643-8679-5_4
