Matches in SemOpenAlex for { <https://semopenalex.org/work/W2953088564> ?p ?o ?g. }
Showing items 1 to 64 of
64
with 100 items per page.
- W2953088564 endingPage "87" @default.
- W2953088564 startingPage "81" @default.
- W2953088564 abstract "3-Substituted N-Boc-1,2-dihydroisoquinolines 2 can be functionalized at the 1-position via lithiation and subsequent electrophilic trapping. The resulting products 3 can be deprotected and oxidized to afford the corresponding 1,3-disubstituted isoquinolines 5. Deprotection of dihydroisoquinoline 3k followed by sodium borohydride reduction affords the cis-1,3-disubstituted tetrahydroisoquinoline 11. The 1,3-disubstituted N-Boc-1,2-dihydroisoquinoline 3g is efficiently alkylated at the 1-position to give 1,1,3-trisubstituted analogs 12." @default.
- W2953088564 created "2019-06-27" @default.
- W2953088564 creator A5037782599 @default.
- W2953088564 creator A5040280722 @default.
- W2953088564 date "1995-01-01" @default.
- W2953088564 modified "2023-09-25" @default.
- W2953088564 title "Preparation of 1,3-disubstituted isoquinoline derivatives fromN-boc-3-substituted-1,2-dihydroisoquinolines" @default.
- W2953088564 cites W1591845898 @default.
- W2953088564 cites W2017670410 @default.
- W2953088564 cites W2031889920 @default.
- W2953088564 cites W2072498442 @default.
- W2953088564 cites W2107904220 @default.
- W2953088564 cites W2363633532 @default.
- W2953088564 cites W2949616338 @default.
- W2953088564 cites W2950589493 @default.
- W2953088564 cites W2952872644 @default.
- W2953088564 cites W989561876 @default.
- W2953088564 doi "https://doi.org/10.1002/jhet.5570320115" @default.
- W2953088564 hasPublicationYear "1995" @default.
- W2953088564 type Work @default.
- W2953088564 sameAs 2953088564 @default.
- W2953088564 citedByCount "2" @default.
- W2953088564 crossrefType "journal-article" @default.
- W2953088564 hasAuthorship W2953088564A5037782599 @default.
- W2953088564 hasAuthorship W2953088564A5040280722 @default.
- W2953088564 hasConcept C161790260 @default.
- W2953088564 hasConcept C164361826 @default.
- W2953088564 hasConcept C178790620 @default.
- W2953088564 hasConcept C185592680 @default.
- W2953088564 hasConcept C21951064 @default.
- W2953088564 hasConcept C2776406546 @default.
- W2953088564 hasConcept C2776923262 @default.
- W2953088564 hasConcept C2780048404 @default.
- W2953088564 hasConcept C50027330 @default.
- W2953088564 hasConceptScore W2953088564C161790260 @default.
- W2953088564 hasConceptScore W2953088564C164361826 @default.
- W2953088564 hasConceptScore W2953088564C178790620 @default.
- W2953088564 hasConceptScore W2953088564C185592680 @default.
- W2953088564 hasConceptScore W2953088564C21951064 @default.
- W2953088564 hasConceptScore W2953088564C2776406546 @default.
- W2953088564 hasConceptScore W2953088564C2776923262 @default.
- W2953088564 hasConceptScore W2953088564C2780048404 @default.
- W2953088564 hasConceptScore W2953088564C50027330 @default.
- W2953088564 hasIssue "1" @default.
- W2953088564 hasLocation W29530885641 @default.
- W2953088564 hasOpenAccess W2953088564 @default.
- W2953088564 hasPrimaryLocation W29530885641 @default.
- W2953088564 hasRelatedWork W1980759909 @default.
- W2953088564 hasRelatedWork W2017670410 @default.
- W2953088564 hasRelatedWork W2019919093 @default.
- W2953088564 hasRelatedWork W2060529417 @default.
- W2953088564 hasRelatedWork W2329822677 @default.
- W2953088564 hasRelatedWork W2949605228 @default.
- W2953088564 hasRelatedWork W2952394827 @default.
- W2953088564 hasRelatedWork W2953157613 @default.
- W2953088564 hasRelatedWork W3008004010 @default.
- W2953088564 hasRelatedWork W3009288646 @default.
- W2953088564 hasVolume "32" @default.
- W2953088564 isParatext "false" @default.
- W2953088564 isRetracted "false" @default.
- W2953088564 magId "2953088564" @default.
- W2953088564 workType "article" @default.