Аннотация:
Based on chiral cyclopentene blocks 2 and 3, enantiomeric cyclosarcomycins 4 and 5 were obtained and characterised.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
A. M. Gimazetdinov, T. V. Gimazetdinova, M. S. Miftakhov, “Synthesis of enantiomeric cyclosarcomycins”, Mendeleev Commun., 20:1 (2010), 15–16
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2975
https://www.mathnet.ru/rus/mendc/v20/i1/p15
Эта публикация цитируется в следующих 7 статьяx:
Xian-Zhang Liao, Ran Wang, Xin Wang, Guang Li, “Enantioselective total synthesis of (‒)-lucidumone enabled by tandem prins cyclization/cycloetherification sequence”, Nat Commun, 15:1 (2024)
A. M. Gimazetdinov, V. V. Zagitov, Z. R. Makaev, “Approaches to the Formation of the Key 2-Oxabicyclo[3.3.0]octan-3-one Precursor of Galiellalactone”, Russ J Org Chem, 60:11 (2024), 2130
Airat M. Gimazetdinov, Aidar Z. Al'mukhametov, Mansur S. Miftakhov, “Development of a new approach for the synthesis of (+)-15-deoxy-Δ12,14-prostaglandin J2 methyl ester based on the [2+2]-cycloadduct of 5-trimethylsilylcyclopentadiene and dichloroketene”, New J. Chem., 46:14 (2022), 6708
A. Z. Al'mukhametov, A. M. Gimazetdinov, M. S. Miftakhov, “Synthetically attractive chiral cyclopentenone building blocks conjugated with tetrahydro- and 2-oxotetrahydrofurans”, Mendeleev Commun., 28:4 (2018), 362–363
Airat M. Gimazetdinov, Nadezhda A. Ivanova, Mansur S. Miftakhov, “A New Approach to the Synthesis of Chiral Blocks for Cyclopentanoids”, Natural Product Communications, 8:7 (2013)
A. M. Gimazetdinov, G. V. Ishmurzina, M. S. Miftakhov, “Sarkomycin A methyl esters and functionalized cyclopentane blocks for brefeldin A”, Russ J Org Chem, 48:1 (2012), 8
Airat M. Gimazetdinov, Tat'yana V. Gimazetdinova, Mansur S. Miftakhov, “ChemInform Abstract: Synthesis of Enantiomeric Cyclosarcomycins.”, ChemInform, 41:25 (2010)