Zobrazeno 1 - 10
of 196
pro vyhledávání: '"DOUGLAS W. YOUNG"'
Publikováno v:
Social Work Research. 39:135-146
The study discussed in this article aimed to explore geographic variation in teen court program completion and recidivism and examine the value of teen courts from the point of view of respondents and their families. Mixed methods, including survival
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c200c74214aab546804d7ee84192e5c
https://doi.org/10.1093/swr/svv018
https://doi.org/10.1093/swr/svv018
Publikováno v:
Tetrahedron. 70:7221-7228
A synthesis of protected homochiral tetrahydropteridines from (2 S )-malic acid has been developed. This presents methodology for the synthesis of reduced pteridine coenzymes and pharmaceuticals.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::145ebbc366297c6ade168f2749c67465
https://doi.org/10.1016/j.tet.2014.06.048
https://doi.org/10.1016/j.tet.2014.06.048
Publikováno v:
ChemInform. 46
The synthesis of protected homochiral tetrahydropteridines with stereochemistry of natural coenzymes at C-6 from (S)-malic acid is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03f1ba05d8c9163f0fabf968c0b3a70d
https://doi.org/10.1002/chin.201509238
https://doi.org/10.1002/chin.201509238
Publikováno v:
Journal of Chemical Research. 2006:580-583
The vinylogous thiazine urethanes 1 are invariably acylated on carbon and not on nitrogen, even when the carbon is “blocked” as in 18. The analogous thiazolidine 2 is acylated either on carbon or nitrogen, depending on the electrophile used.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37e5f2525011055850f442df6c575ad9
https://doi.org/10.3184/030823406778521365
https://doi.org/10.3184/030823406778521365
Publikováno v:
European Journal of Biochemistry. 5/2/77, Vol. 75 Issue 1, p133-147. 15p.
Publikováno v:
Tetrahedron Letters. 46:2093-2096
Trimethyl (2S,3R)- and (2R,3R)-[2-H-2(1)]-homocitrates, 10b and 10c respectively, and dimethyl (2S,3R)- and (2R,3R)[2 [2-H-2(1)]-homocitric lactones, 11b and 11c respectively, have been synthesised from shikimic acid and [2-H-2]-shikimic acid by a ro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d37c604474e565a75a1e85aee36f025d
https://doi.org/10.1016/j.tetlet.2005.01.134
https://doi.org/10.1016/j.tetlet.2005.01.134
Publikováno v:
Tetrahedron. 61:301-312
The (3S,6S,10S)-7/5 bicyclic lactam 4, designed as an external turn constraint, was synthesised by a new stereoselective route involving Eschenmoser condensation. Calculated preferred conformations compare well with the preferred solid state conforma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86a3f55133227ac4193a85c1ec8def8c
https://doi.org/10.1016/j.tet.2004.09.037
https://doi.org/10.1016/j.tet.2004.09.037
Publikováno v:
Tetrahedron. 61:287-299
Two external β-turn templates have been synthesised and one of them has been derivatised as a GLDV-tetrapeptide. In the course of the synthesis an interesting dichotomy was observed in the condensation of exocyclic enamines such as 4 and 19 with pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81946fc3505b48ec220d367a4f8ff1e7
https://doi.org/10.1016/j.tet.2004.09.036
https://doi.org/10.1016/j.tet.2004.09.036
Publikováno v:
Org. Biomol. Chem.. 2:1310-1314
A new synthesis of (2S,3R)-[3′,3′,3′-2H3]-valine 2 has been completed and (2S,3S)-4-fluorovaline 4 has been synthesised for the first time. Both compounds have been prepared by routes involving stereoselective addition to the (S)-pyroglutamate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19babce2b69b3eeea1558d4f2545097d
https://doi.org/10.1039/b401646g
https://doi.org/10.1039/b401646g
Autor:
David E. Davies, Paul M. Doyle, R.Duncan Farrant, Richard D. Hill, Peter B. Hitchcock, Paul N. Sanderson, Douglas W. Young
Publikováno v:
Tetrahedron Letters. 44:8887-8891
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1ba42fbba6d2b57678aa4917329dc4a
https://doi.org/10.1016/j.tetlet.2003.09.170
https://doi.org/10.1016/j.tetlet.2003.09.170