Matches in SemOpenAlex for { <https://semopenalex.org/work/W3099661330> ?p ?o ?g. }
Showing items 1 to 52 of
52
with 100 items per page.
- W3099661330 abstract "Chaozhong Li of the Shanghai Institute of Organic Chemistry demonstrated (Organic Lett. 2008, 10, 4037) facile and selective Cu-catalyzed β-lactam formation, converting 1 to 2. Paul Helquist of the University of Notre Dame devised (Organic Lett. 2008, 10, 3903) an effective catalyst for intramolecular alkyne hydroamination, converting 3 into the imine 4. Six-membered ring construction worked well also. Jon T. Njardarson of Cornell University found (Organic Lett. 2008, 10, 5023) a Cu catalyst for the rearrangement of alkenyl aziridines such as 5 to the pyrroline 6. Philippe Karoyan of the UPMC, Paris developed (J. Org. Chem. 2008, 73, 6706) an interesting chiral auxiliary directed cascade process, converting the simple precursor 7 into the complex pyrrolidine 9. Sherry R. Chemler of the State University of New York, Buffalo devised (J. Am. Chem. Soc. 2008, 130, 17638) a chiral Cu catalyst for the cyclization of 10, to give 12 with substantial enantiocontrol. Wei Wang of the University of New Mexico demonstrated (Chem. Commun. 2008, 5636) the organocatalyzed condensation of 13 and 14 to give 16 with high enantio- and diastereocontrol. Two complementary routes to azepines/azepinones have appeared. F. Dean Toste of the University of California, Berkeley showed (J. Am. Chem. Soc. 2008, 130, 9244) that a gold complex catalyzed the condensation of 17 and 18 to give 19. Frederick G. West of the University of Alberta found (Organic Lett. 2008, 10, 3985) that lactams such as 20 could be ring-expanded by the addition of the propiolate anion 21. Takeo Kawabata of Kyoto University extended (Organic Lett . 2008, 10, 3883) “memory of chirality” studies to the cyclization of 23, demonstrating that 24 was formed in high ee. Paul V. Murphy of University College Dublin took advantage (Organic Lett . 2008, 10, 3777) of the well-known intramolecular addition of azides to alkenes, showing that the intermediate could be intercepted with nucleophiles such as thiophenol, to give the cyclized product 26 with high diastereocontrol." @default.
- W3099661330 created "2020-11-23" @default.
- W3099661330 creator A5052375923 @default.
- W3099661330 date "2011-10-13" @default.
- W3099661330 modified "2023-09-27" @default.
- W3099661330 title "New Methods for C-N Ring Construction" @default.
- W3099661330 doi "https://doi.org/10.1093/oso/9780199764549.003.0055" @default.
- W3099661330 hasPublicationYear "2011" @default.
- W3099661330 type Work @default.
- W3099661330 sameAs 3099661330 @default.
- W3099661330 citedByCount "0" @default.
- W3099661330 crossrefType "book-chapter" @default.
- W3099661330 hasAuthorship W3099661330A5052375923 @default.
- W3099661330 hasConcept C155647269 @default.
- W3099661330 hasConcept C161790260 @default.
- W3099661330 hasConcept C178790620 @default.
- W3099661330 hasConcept C185592680 @default.
- W3099661330 hasConcept C188027245 @default.
- W3099661330 hasConcept C2776573223 @default.
- W3099661330 hasConcept C2778851528 @default.
- W3099661330 hasConcept C2780378348 @default.
- W3099661330 hasConcept C71240020 @default.
- W3099661330 hasConcept C75079739 @default.
- W3099661330 hasConcept C7596914 @default.
- W3099661330 hasConceptScore W3099661330C155647269 @default.
- W3099661330 hasConceptScore W3099661330C161790260 @default.
- W3099661330 hasConceptScore W3099661330C178790620 @default.
- W3099661330 hasConceptScore W3099661330C185592680 @default.
- W3099661330 hasConceptScore W3099661330C188027245 @default.
- W3099661330 hasConceptScore W3099661330C2776573223 @default.
- W3099661330 hasConceptScore W3099661330C2778851528 @default.
- W3099661330 hasConceptScore W3099661330C2780378348 @default.
- W3099661330 hasConceptScore W3099661330C71240020 @default.
- W3099661330 hasConceptScore W3099661330C75079739 @default.
- W3099661330 hasConceptScore W3099661330C7596914 @default.
- W3099661330 hasLocation W30996613301 @default.
- W3099661330 hasOpenAccess W3099661330 @default.
- W3099661330 hasPrimaryLocation W30996613301 @default.
- W3099661330 hasRelatedWork W1993282154 @default.
- W3099661330 hasRelatedWork W2058333778 @default.
- W3099661330 hasRelatedWork W2063633419 @default.
- W3099661330 hasRelatedWork W2097939669 @default.
- W3099661330 hasRelatedWork W2122333470 @default.
- W3099661330 hasRelatedWork W2143350172 @default.
- W3099661330 hasRelatedWork W2949770424 @default.
- W3099661330 hasRelatedWork W2949781101 @default.
- W3099661330 hasRelatedWork W2950274702 @default.
- W3099661330 hasRelatedWork W2952744990 @default.
- W3099661330 isParatext "false" @default.
- W3099661330 isRetracted "false" @default.
- W3099661330 magId "3099661330" @default.
- W3099661330 workType "book-chapter" @default.