Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Gidget C. Tay"'
Publikováno v:
Organic Letters. 18:3050-3053
Progress toward understanding the scope and diastereoselectivity of intramolecular Diels-Alder reactions using 2-cyano-1-azadienes is described herein. The resulting cyanoenamine products are underutilized intermediates in organic synthesis. Assembly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83cacd0e3f5a90a5f086ac991a30e605
https://doi.org/10.1021/acs.orglett.6b00881
https://doi.org/10.1021/acs.orglett.6b00881
Autor:
Kimberly D. Edwards, Gidget C. Tay
Publikováno v:
Journal of Chemical Education. 92:1956-1959
A visual aid teaching tool, the DanceChemistry video series, has been developed to teach fundamental chemistry concepts through dance. These educational videos portray chemical interactions at the molecular level using dancers to represent chemical s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab374ae90f61337f7dc5c54e3d15cac5
https://doi.org/10.1021/acs.jchemed.5b00315
https://doi.org/10.1021/acs.jchemed.5b00315
Publikováno v:
The Journal of Organic Chemistry
The Journal of organic chemistry, vol 79, iss 18
Tay, GC; Huang, CY; & Rychnovsky, SD. (2014). Silyl enol ether Prins cyclization: Diastereoselective formation of substituted tetrahydropyran-4-ones. Journal of Organic Chemistry, 79(18), 8733-8749. doi: 10.1021/jo501580p. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/3r93f7fj
The Journal of organic chemistry, vol 79, iss 18
Tay, GC; Huang, CY; & Rychnovsky, SD. (2014). Silyl enol ether Prins cyclization: Diastereoselective formation of substituted tetrahydropyran-4-ones. Journal of Organic Chemistry, 79(18), 8733-8749. doi: 10.1021/jo501580p. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/3r93f7fj
© 2014 American Chemical Society. A diastereoselective synthesis of cis-2,6-disubstituted tetrahydropyran-4-ones was developed. The key step of this methodology, a silyl enol ether Prins cyclization, was promoted by a condensation reaction between a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c40973d850b6fc16a885b9d8cae3b1d1
https://doi.org/10.1021/jo501580p
https://doi.org/10.1021/jo501580p
Publikováno v:
ChemInform. 47
Progress toward understanding the scope and diastereoselectivity of intramolecular Diels–Alder reactions using 2-cyano-1-azadienes is described herein. The resulting cyanoenamine products are underutilized intermediates in organic synthesis. Assemb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f6d9cf4b99b4273f9e2cacbb6a29fc9
https://doi.org/10.1002/chin.201646169
https://doi.org/10.1002/chin.201646169
Publikováno v:
ChemInform. 46
The corresponding starting compounds are prepared in a 4 step sequence via weinreb amide intermediates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf1013a456031a2238b80611fc3a953a
https://doi.org/10.1002/chin.201512197
https://doi.org/10.1002/chin.201512197
Publikováno v:
ChemInform. 45
The condensation of α-hydroxy silyl enol ethers with aldehydes is optimized in order to synthesize 2,6-disubstituted 3,3-dimethyltetrahydropyran-4-ones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fd4094568545693a5ddc8dec90d3bbd
https://doi.org/10.1002/chin.201405136
https://doi.org/10.1002/chin.201405136