One-Pot Synthesis of 3,4-Dihydropyrimidino[2,1-a]isoindol-6(2H)-one
- Авторлар: Martyanov G.S1, Barabanov M.A1, Pestov A.V1
-
Мекемелер:
- Postovsky Institute of Organic Synthesis UB RAS
- Шығарылым: Том 61, № 6 (2025)
- Беттер: 721-727
- Бөлім: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://journals.rcsi.science/0514-7492/article/view/355702
- DOI: https://doi.org/10.7868/S3034630425060095
- ID: 355702
Дәйексөз келтіру
Аннотация
Авторлар туралы
G. Martyanov
Postovsky Institute of Organic Synthesis UB RAS
ORCID iD: 0000-0002-5850-8443
Ekaterinburg, Russia
M. Barabanov
Postovsky Institute of Organic Synthesis UB RAS
Email: filmsey@mail.ru
ORCID iD: 0009-0000-1152-0317
Ekaterinburg, Russia
A. Pestov
Postovsky Institute of Organic Synthesis UB RAS
ORCID iD: 0000-0002-4270-3041
Ekaterinburg, Russia
Әдебиет тізімі
- Ettlinger M., Hodgkins J. J. Am. Chem. Soc., 1955, 77, 1831–1836. doi: 10.1021/ja01612a035
- Beaton G., Moree W.J., Rueter J.K., Dahl R.S., Meelligott D.L., Goldman P., Demaggio A.J., Christenson E., Herendeen D., Fowler K.W., Huang D., Bertino J.A., Bourdon L.H., Fairfax D.J., Jiang Q., Reisch H.A., Song R.H., Zhichkin P.E. WO 2003 015785 (2003). Cd, 2003, 138, 205069.
- Iwata M., Kuzuhara H. Bull. Chem. Soc. Jpn., 1989, 62, 198–210. doi: 10.1246/bcsj.62.198
- Houlihan W.J., Kelly L., Pankuch J., Koletar J., Brand L., Janowsky A., Kopajic T.A. J. Med. Chem., 2002, 45, 4097–4109. doi: 10.1021/jm010302r
- Ravu R.R., Jacob M.R., Khan S.I., Wang M., Cao L., Agarwal A.K., Clarek A. M., Li X.-C. J. Nat. Prod., 2021, 84, 2129–2199. doi: 10.1021/acs.jnatprod.1c00116
- Plowman J., Pauli K., Atassi G., Harrison S., Dykes D., Kabbe H., Narayanan V.L., Yoder O. Invest. New Drugs, 1988, 6, 147–153. doi: 10.1007/BF00175391
- Rao V.A., Agama K., Holbeck S., Pommiert Y. Cancer Res., 2007, 20, 9971–9979. doi: 10.1158/0008-5472.CAN-07-0804
- Martyanov G.S., Barabanov M.A., Pestov A.V. XIII Int. Conf. Chem. Young Sci. "Mendeleev 2024", St. Petersburg: VVM Publishing LLC, 2024, 473. https://drive.google.com/file/d/1DyY-C1-Dop22VZNWDAMRNQG_e38a3HUL/view
- Tequi P., Peano A., Decuupere M., Gibbs A., Kleijwegt P., Muhla S., Le Deore C., Yifru A. WO 2022 259193 (2022). Cd, 2022, 181, 91453.
- Nakamura A., Takamoto K. Pat. 4130075 (2008). Japan. Cd, 2008, 139, 53036.
- Eguchi S., Takeuchi H. J. Chem. Soc., Chem. Commun., 1989, 9, 602–603. doi: 10.1039/C39890000602
- Gaozza C.H., Grinberg H., Lamdan S. J. Heterocycl. Chem., 1972, 9, 883–886. doi: 10.1002/jhet.5570090422
- Spiessens L. I., Anteunis M. J. O. Bull. Soc. Chim. Belg., 1983, 92, 965–993. doi: 10.1002/bscb.19830921107
- Veznik F., Guggisberg A., Hesse M. Helv. Chim. Acta, 1991, 74, 654–661. doi: 10.1002/hlca.19910740322
- Kraus M.A. Synthesis, 1973, 6, 361–362. doi: 10.1055/s-1973-22217
- Atkins P.W., de Paula J. Phys. Chem. Life Sci., 3rd ed., Oxford Univ. Press, Oxford, 2006. doi: 10.1093/hessc/9780198830108.001.0001
- Sulkowski T.S. Pat. 3507867 (1968). USA. C4, 1968, 74, 757774.
Қосымша файлдар

