Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Michael D. Weller"'
Autor:
Michael D. Weller, Nigel S. Simpkins
Publikováno v:
Tetrahedron Letters. 51:4823-4826
The tricyclic natural products ialibinone A and ialibinone B were prepared as a 41:59 mixture in four steps starting from phloroglucinol. The synthetic sequence involved (i) acylation of phloroglucinol under Friedel–Crafts conditions, (ii) double p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::872da9a2dc3303df4993067acbdfa9c4
https://doi.org/10.1016/j.tetlet.2010.07.025
https://doi.org/10.1016/j.tetlet.2010.07.025
Autor:
Nigel S. Simpkins, Michael D. Weller
Publikováno v:
Stereochemical Aspects of Organolithium Compounds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0977040f62c18232dffbaf7c53c69035
https://doi.org/10.1002/9783906390628.ch1
https://doi.org/10.1002/9783906390628.ch1
Publikováno v:
The Journal of Organic Chemistry. 74:7898-7907
A two-directional synthesis of a masked hexayne 7, in which two beta-chlorovinylsilanes protect two of the internal alkynes, is reported. The key step involves the Pd-catalyzed oxidative dimerization of alkyne 10 to provide diyne 12, which is elabora
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef0fb8d9e1024a2a85a9d8899d3cc116
https://doi.org/10.1021/jo901766p
https://doi.org/10.1021/jo901766p
Autor:
Liam R. Cox, Michael D. Weller
Publikováno v:
Comptes Rendus Chimie. 12:366-377
This article summarises our recent efforts towards using β-halovinylsilanes in a new approach to oligoyne assembly. β-Halovinylsilanes are particularly useful masked alkynes since the free alkyne can be released under mild reaction conditions by tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::401a908c96976cd5d215ac7622141028
https://doi.org/10.1016/j.crci.2008.09.027
https://doi.org/10.1016/j.crci.2008.09.027
Publikováno v:
Tetrahedron Letters. 49:4596-4600
A stereoselective halodestannylation of (E)-β-stannylvinylsilane 6 has been used to access a range of (E)-β-halovinylsilanes. Most notably, the β-fluorovinylsilane 14 was accessed in high yield using the Selectfluor® reagent, and subsequently con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dea44d7892d113744332c53bbccdb2b
https://doi.org/10.1016/j.tetlet.2008.05.081
https://doi.org/10.1016/j.tetlet.2008.05.081
Autor:
Michael D. Weller, Nigel S. Simpkins
Publikováno v:
ChemInform. 45
Lithium dialkylamides, especially lithium diisopropylamide (LDA), are valuable bases in organic synthesis but it is only since 1980 that their chiral counterparts have found application in reactions that can be broadly defined as asymmetric deprotona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4816555e6b9d0041c42827925e44849e
https://doi.org/10.1002/chin.201421252
https://doi.org/10.1002/chin.201421252
Publikováno v:
ChemInform. 44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::313d3e20a1a5107886da8c32eddbf1f2
https://doi.org/10.1002/chin.201348200
https://doi.org/10.1002/chin.201348200
Publikováno v:
Organicbiomolecular chemistry. 11(30)
A strategy for the synthesis of members of the prenylated indole alkaloid family is described, which involves a radical cascade process of an appropriately substituted diketopiperazine (DKP) core structure. Several approaches to the generation of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac8b0f3132e1d24dcf24e40a17bec240
https://pubmed.ncbi.nlm.nih.gov/23797367
https://pubmed.ncbi.nlm.nih.gov/23797367
Autor:
Nigel S. Simpkins, Michael D. Weller
Publikováno v:
Organic Reactions
Lithium dialkylamides, especially lithium diisopropylamide (LDA), are valuable bases in organic synthesis but it is only since 1980 that their chiral counterparts have found application in reactions that can be broadly defined as asymmetric deprotona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::448912a510f8b6d1d39f91196742559d
https://doi.org/10.1002/0471264180.or079.02
https://doi.org/10.1002/0471264180.or079.02
Autor:
Michael D. Weller, Liam R. Cox
Publikováno v:
ChemInform. 41
This article summarises our recent efforts towards using β-halovinylsilanes in a new approach to oligoyne assembly. β-Halovinylsilanes are particularly useful masked alkynes since the free alkyne can be released under mild reaction conditions by tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e1593e4cfaea48ed56d69fe7cd68a5a
https://doi.org/10.1002/chin.201014220
https://doi.org/10.1002/chin.201014220