Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Toms Kalnins"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:586-602
Aliphatic alkyl chain-containing 12–14-membered macrocycles have been designed as structural analogs of antimitotic natural product diazonamide A. Macrocycles were synthesized from 5-bromooxazole in 7 to 9 linear steps using Ru-catalyzed ring-closi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cf9c073d229c1da3fbf929eb97ae312
https://doi.org/10.1007/s10593-020-02704-6
https://doi.org/10.1007/s10593-020-02704-6
Publikováno v:
Chemistry of Heterocyclic Compounds. 51:613-620
Benzofuro[2,3-b]indolines undergo ring opening in the presence of base to generate 3H-indolines. The latter can rearrange into 3-arylindoles through an intramolecular transfer of the methoxycarbonyl moiety from quaternary carbon to oxygen of phenol.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::959f9c789410376ace96893bb8997af6
https://doi.org/10.1007/s10593-015-1749-7
https://doi.org/10.1007/s10593-015-1749-7
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:1501-1505
How to Cite Kinens, A.; Kalnins, T.; Suna E. Chem. Heterocycl. Compd. 201 5 , 50 , 1501. [ Khim. Geterotsikl. Soedin. 2014 , 1629.] For this article in the English edition see DOI 10.1007/s10593-014-1616-y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04f2a9d9c3e641824d42a136e5ede726
https://doi.org/10.1007/s10593-014-1616-y
https://doi.org/10.1007/s10593-014-1616-y
Publikováno v:
The Journal of Organic Chemistry. 79:3715-3724
Hydroxymethylation of cyclic tert-butanesulfinylketimine-derived lithium enamides with methoxymethanol proceeds with excellent diastereoselectivity (99:1 dr). Methoxymethanol is a stable and easy-to-handle source of anhydrous monomeric formaldehyde i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90ad03f81a1aa4ec0f528115af116f1d
https://doi.org/10.1021/jo500506u
https://doi.org/10.1021/jo500506u
Publikováno v:
ChemInform. 46
A previously unknown formation of acridines from triarylcarbinols under acidic conditions via a two-step ortho-lithiation cyclization sequence is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0e94c1bac55ceafc25503b412e9de54
https://doi.org/10.1002/chin.201526200
https://doi.org/10.1002/chin.201526200
Publikováno v:
The Journal of organic chemistry. 80(6)
Stereoselective synthesis of the right-hand heteroaromatic macrocycle of diazonamide A features C16–C18 bond formation in the Suzuki–Miyaura cross-coupling and atropodiastereoselective Dieckmann-type macrocyclization as key steps. The Suzuki–Mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a3ae79de750a9d32575dccd532c5412
https://pubmed.ncbi.nlm.nih.gov/25705925
https://pubmed.ncbi.nlm.nih.gov/25705925
Publikováno v:
ChemInform. 45
Hydroxymethylation of cyclic tert-butanesulfinylketimine-derived lithium enamides with methoxymethanol proceeds with excellent diastereoselectivity (99:1 dr). Methoxymethanol is a stable and easy-to-handle source of anhydrous monomeric formaldehyde i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13d13fd4c59b16f85fd1c23b6712ecb4
https://doi.org/10.1002/chin.201442038
https://doi.org/10.1002/chin.201442038