Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kenneth S. Matthews"'
Autor:
Kenneth S. Matthews, Philip Magnus
Publikováno v:
Tetrahedron. 68:6343-6360
A divergent synthesis to the tetrahydroisoquinoline alkaloids (±)-renieramycin G and (±)-lemonomycinone amide is reported. A strategy was developed that allowed access to both the diazabicyclo[3.3.1]nonane and diazabicyclo[3.2.1]octane ring systems
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18bb49cb741a134cb69d7f28c64c1f38
https://doi.org/10.1016/j.tet.2012.02.043
https://doi.org/10.1016/j.tet.2012.02.043
Publikováno v:
The Journal of Organic Chemistry. 63:8432-8439
New guanidinylation reagents are reported. These reagents consist of N,N‘,N‘‘-tri-Boc-guanidine (1) and N,N‘,N‘‘-tri-Cbz-guanidine (2), which allow for the facile conversion of alcohols to substituted guanidines. A series of arginine anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c42bf5d116a91b119f55cd3912d8b186
https://doi.org/10.1021/jo9814344
https://doi.org/10.1021/jo9814344
Publikováno v:
ChemInform. 30
New guanidinylation reagents are reported. These reagents consist of N,N‘,N‘‘-tri-Boc-guanidine (1) and N,N‘,N‘‘-tri-Cbz-guanidine (2), which allow for the facile conversion of alcohols to substituted guanidines. A series of arginine anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a6557e86232c21a4b639e50229b83fa
https://doi.org/10.1002/chin.199915232
https://doi.org/10.1002/chin.199915232
Autor:
Kenneth S. Matthews, Philip Magnus
Publikováno v:
ChemInform. 37
The total synthesis of tetrahydroisoquinoline alkaloids (+/-)-renieramycin G (4) and a lemonomycinone analogue (7) is described. A general strategy to synthesize both the mono- and bistetrahydroisoquinoline alkaloids from a common advanced intermedia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d50c1409ad40f35b6deaceacc0f74a6
https://doi.org/10.1002/chin.200604192
https://doi.org/10.1002/chin.200604192
Publikováno v:
ChemInform. 34
A general strategy for the formation of 1,3-cis-substituted tetrahydroisoquinolines is described from ortho-iodo imines involving Larock isoquinoline synthesis, addition of organolithium compounds to unactivated isoquinolines, and ionic hydrogenation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::211220733de50e1e09ff64c0c4bbb02f
https://doi.org/10.1002/chin.200340151
https://doi.org/10.1002/chin.200340151
Publikováno v:
Organic letters. 5(12)
[reaction: see text] A general strategy for the formation of 1,3-cis-substituted tetrahydroisoquinolines is described from ortho-iodo imines involving Larock isoquinoline synthesis, addition of organolithium compounds to unactivated isoquinolines, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3cf270392772b2b536c74a573ad200a4
https://pubmed.ncbi.nlm.nih.gov/12790559
https://pubmed.ncbi.nlm.nih.gov/12790559