Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ondřej, Kováč"'
Publikováno v:
The Journal of Organic Chemistry. 86:11291-11309
In this paper, we report a unified approach to N-substituted and N,N-disubstituted benzothiazole (BT) sulfonamides. Our approach to BT-sulfonamides starts from simple commercially available building blocks (benzo[d]thiazole-2-thiol and primary and se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec7e0ff8fb57f6f19dc49877f6626993
https://doi.org/10.1021/acs.joc.1c00317
https://doi.org/10.1021/acs.joc.1c00317
Autor:
Ondřej Kováč, David J.-Y.D. Bon, František Zálešák, Lukas Roiser, Lubomír Vojtěch Baar, Mario Waser, Jiri Pospisil
Publikováno v:
The Journal of Organic Chemistry. 85:7192-7206
In this paper, we report the formation of highly electrophilic 1,1-deactivated olefins, their use as novel synthetic building blocks, and their transformation to structurally diverse molecular scaf...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39e613deb53ff6f37b68c0e7e879f482
https://doi.org/10.1021/acs.joc.0c00571
https://doi.org/10.1021/acs.joc.0c00571
Publikováno v:
The Journal of organic chemistry. 86(17)
In this paper, we report a unified approach to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::132837503518d8e26d80314467785368
https://pubmed.ncbi.nlm.nih.gov/34479409
https://pubmed.ncbi.nlm.nih.gov/34479409
Autor:
Ondřej, Kováč, František, Zálešák, David, J-Y D Bon, Lukas, Roiser, Lubomír V, Baar, Mario, Waser, Jiří, Pospíšil
Publikováno v:
The Journal of organic chemistry. 85(11)
In this paper, we report the formation of highly electrophilic 1,1-deactivated olefins, their use as novel synthetic building blocks, and their transformation to structurally diverse molecular scaffolds. Synthesis of 1,1-deactivated olefins substitut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed65c947c08a76844196422771520a84
https://pubmed.ncbi.nlm.nih.gov/32352285
https://pubmed.ncbi.nlm.nih.gov/32352285
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany)
The first highly asymmetric catalytic synthesis of densely functionalized dihydrobenzofurans is reported, which starts from ortho-hydroxy-containing para-quinone methides. The reaction relies on an unprecedented formal [4+1]-annulation of these quino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d6ea270b68345e2a73826a89e949cd51
https://pubmed.ncbi.nlm.nih.gov/31020717
https://pubmed.ncbi.nlm.nih.gov/31020717
Publikováno v:
The Journal of organic chemistry. 83(9)
Herein we report the efficient one- and two-carbon homologation of 1° and 2° alcohols to their corresponding homologated esters via the Mitsunobu reaction using β-carbonyl benzothiazole (BT) sulfone intermediates. The one-carbon homologation appro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f228a9d76909a025e1312f686a8d22d1
https://pubmed.ncbi.nlm.nih.gov/29667824
https://pubmed.ncbi.nlm.nih.gov/29667824