Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Brian G. Pujanauski"'
Publikováno v:
Organic Letters. 14:648-651
A rapid synthesis of the tetracyclic core of Kopsia indole alkaloids related to lapidilectine B, grandilodine C, and tenuisine A is reported. Key to the success of this route was an efficient and scalable Ugi four-component coupling to install all th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5359ac15618d2a6ae952620a580996d9
https://doi.org/10.1021/ol203302f
https://doi.org/10.1021/ol203302f
Publikováno v:
Tetrahedron. 62:4715-4727
We report a method for the efficient construction of small molecule macroarrays using microwave-assisted SPOT-synthesis. Macroarrays of 1,3-diphenylpropenones (chalcones) were synthesized rapidly and in high purity starting from robust, Wang-linker-d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89f5e4772128bf43b95621a66b6eff6a
https://doi.org/10.1016/j.tet.2006.02.083
https://doi.org/10.1016/j.tet.2006.02.083
Publikováno v:
Organic letters. 11(14)
A general approach to the tetracyclic core of the neomangicol natural products via a late-stage indene alkylation reaction is presented. This strategy sets the stage for access to the neomangicol family and, in addition, provides a potential biogenet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::979b0c689ca7e2d1c5ffe5996bd4737b
https://pubmed.ncbi.nlm.nih.gov/19527042
https://pubmed.ncbi.nlm.nih.gov/19527042
Publikováno v:
Analytical chemistry. 80(13)
Selective noncovalent adduct protein probing (SNAPP) mass spectrometry was recently developed to study solution-phase conformations of proteins by exploiting the specific affinity between 18-crown-6 ether (18C6) and lysine side chains. To obtain more
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b48ce783b14b79af6059f1e688b5a9c
https://pubmed.ncbi.nlm.nih.gov/18498182
https://pubmed.ncbi.nlm.nih.gov/18498182
Publikováno v:
ChemInform. 37
A Pt-catalyzed pentannulation of propargylic esters containing an epoxide moiety has been developed. The present transformation achieves the formation of cyclopentenone products as single diastereomers in good yields. The observed products likely for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c9b18cbeefb281ac0f30724ca66fcf1
https://doi.org/10.1002/chin.200639114
https://doi.org/10.1002/chin.200639114
Publikováno v:
Organic Letters; Jan2012, Vol. 14 Issue 2, p648-651, 4p