Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Diterpenoid synthesis"'
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 9, Pp o690-o691 (2015)
The title hydrate, C17H28O2·H2O, was synthesized in order to determine the relative configuration of the tetracyclic framework. The fused 5,6,7-tricarbocyclic core exhibits an entire cis-annulation, featuring a 1,4-cis-relation of the angular methyl
Externí odkaz:
https://doaj.org/article/ee553cd1c35846e4ac0d4f803aeef226
Autor:
Edward Piers, Li Ren
Publikováno v:
Tetrahedron Letters. 53:3329-3332
The first total synthesis of (+)-pentandranoic acid A (1) was accomplished in 14 steps, starting from alcohol 3. Our synthesis features several key transformations, such as an ozonolysis-aldol cyclization-dehydration ring contraction sequence and a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a38fd2d2dbd8ce95d21ad4b054333149
https://doi.org/10.1016/j.tetlet.2012.04.080
https://doi.org/10.1016/j.tetlet.2012.04.080
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 71, Iss 9, Pp o690-o691 (2015)
Acta Crystallographica Section E: Crystallographic Communications
Acta Crystallographica Section E: Crystallographic Communications
The title hydrate, C17H28O2·H2O, was synthesized in order to determine the relative configuration of the tetracyclic framework. The fused 5,6,7-tricarbocyclic core exhibits an entirecis-annulation, featuring a 1,4-cis-relation of the angular methyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eb5b4b6841dc3ca597f4bbdf40dceae
http://scripts.iucr.org/cgi-bin/paper?S2056989015015698
http://scripts.iucr.org/cgi-bin/paper?S2056989015015698
Autor:
Robert J. Barkovich, James C. Liao
Publikováno v:
Metabolic Engineering. 3:27-39
The metabolic engineering of natural products has begun to prosper in the past few years due to genomic research and the discovery of biosynthetic genes. While the biosynthetic pathways and genes for some isoprenoids have been known for many years, n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f95c0d3028c16d0f36a1bf143a48aec4
https://doi.org/10.1006/mben.2000.0168
https://doi.org/10.1006/mben.2000.0168
Publikováno v:
ChemInform. 43
The conversion of oridonin (I) to spirolactone-type (III) or enmein-type diterpenoid (VI) and (VII) is conducted as well as spirolactone-type diterpenoid to enmein-type diterpenoid.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72c795edf280c39e6d1ef54a658de5ad
https://doi.org/10.1002/chin.201239202
https://doi.org/10.1002/chin.201239202
Publikováno v:
Tetrahedron. 49:8233-8240
Tricyclic cyclohexa-2,4-dienones and methylenecyclohexadienes which are potentially useful for diterpenoid synthesis have been prepared by cyclisation of 1,3,5-hexatriene-1-ones and 1,2,4,6-heptatetraenes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8623e94e0736043881d745dab919e610
https://doi.org/10.1016/s0040-4020(01)88041-8
https://doi.org/10.1016/s0040-4020(01)88041-8
Publikováno v:
ChemInform. 25
Tricyclic cyclohexa-2,4-dienones and methylenecyclohexadienes which are potentially useful for diterpenoid synthesis have been prepared by cyclisation of 1,3,5-hexatriene-1-ones and 1,2,4,6-heptatetraenes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49044c8d4b544af35ce1dcedd47ae1f9
https://doi.org/10.1002/chin.199402076
https://doi.org/10.1002/chin.199402076
Akademický článek
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Akademický článek
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Publikováno v:
Bulletin of the Chemical Society of Japan. 52:608-613
A stereocontrolled synthetic route to (±)-1,2,3,4,4a,9,10,10a-octahydro-7-methoxy-1,4a-dimethyl-10-oxophenanthrene-1β-carboxylic acid and its conversion to 1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-10β-hydroxy-1,4a-dimethyl-7-oxophenanthrene-1β-ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da604a8d5d83e4bcc34cc8a8efdf8c94
https://doi.org/10.1246/bcsj.52.608
https://doi.org/10.1246/bcsj.52.608