Zobrazeno 1 - 10
of 77
pro vyhledávání: '"FISCHER projection"'
Autor:
KOTHA, Sambasivarao1 srk@chem.iitb.ac.in, ALI, Rashid1
Publikováno v:
Turkish Journal of Chemistry. 2015, Vol. 39 Issue 6, p1190-1198. 9p.
Publikováno v:
IEEE Transactions on Applied Superconductivity. Jun2018, Vol. 28 Issue 4, p1-5. 5p.
Autor:
MOORI, J.1 Jamshid.Moori@nwu.ac.za, SERETLO, T.1 Thekiso.Seretlo@uniwest.ac.za
Publikováno v:
Bulletin of the Iranian Mathematical Society. 2013, Vol. 39 Issue 5, p1037-1052. 16p. 6 Charts.
Autor:
Gövdeli, Nezafet1, Karakaş, Duran1 dkarakas@cumhuriyet.edu.tr
Publikováno v:
Journal of Molecular Structure. Jul2018, Vol. 1163, p94-102. 9p.
Autor:
T. V. Danylova, S. V. Komisarenko
Publikováno v:
The Ukrainian Biochemical Journal, Vol 90, Iss 4, Pp 135-142 (2018)
Modern biochemistry and molecular biology would be impossible without discoveries in related fields of science. This paper aims to outline briefly the main stages of scientific activity of a Nobel Prize winner 1902 – German chemist Hermann Emil Fis
Externí odkaz:
https://doaj.org/article/efa876e590c947bdb46bff6f7a3c38f4
Autor:
Bezuidenhout, Daniela I.1 daniela.bezuidenhout@up.ac.za, van der Westhuizen, Belinda1, Rosenthal, Amos J.2, Wörle, Michael2, Liles, David C.1, Fernández, Israel3 israel@quim.ucm.es
Publikováno v:
Dalton Transactions: An International Journal of Inorganic Chemistry. 2014, Vol. 43 Issue 2, p398-401. 4p.
Autor:
Mangabeira Júnior, Aldemir Soares, Oliveira Sávio, Karin Eleonora, Pineli, Livia de Lacerda de Oliveira, Akutsu, Rita de Cássia Coelho, Assunção Botelho, Raquel Braz
Publikováno v:
Journal of Culinary Science & Technology; 2018, Vol. 16 Issue 2, p165-177, 13p, 2 Charts
Push, Pivot, and Pull Your Way to Converting Fischer Projections into Staggered Bond-Line Structures
Autor:
Sean C. Butler
Publikováno v:
Journal of Chemical Education. 98:2132-2137
Interconverting different molecular representations can be problematic for many organic chemistry students. This is certainly the case when converting Fischer projections into bond-line structures. When performing the conversion from a Fischer projec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae9897a2bd89bfa25337f2d4b20b3de4
https://doi.org/10.1021/acs.jchemed.1c00006
https://doi.org/10.1021/acs.jchemed.1c00006
Autor:
Sean C. Butler
Publikováno v:
Journal of Chemical Education. 98:678-681
Undergraduate organic chemistry students, as they study conformational analysis and stereochemistry, frequently have trouble manipulating three-dimensional structures on a two-dimensional page or screen. The inability to accurately convert three-dime
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37a7d42ccd288ea0e1556c106f8f7f0d
https://doi.org/10.1021/acs.jchemed.0c01201
https://doi.org/10.1021/acs.jchemed.0c01201
Autor:
Torsten Schmiermund
Publikováno v:
essentials ISBN: 9783658320348
Sugars are among the most important carbohydrates. At this chapter, you will learn what anomers are and in what many different ways (e.g., Fischer projection or Haworth ring formula), sugar molecules can be represented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd50720f90c0ded0717b98171de5eb0b
https://doi.org/10.1007/978-3-658-32035-5_7
https://doi.org/10.1007/978-3-658-32035-5_7
