Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rodney H. White"'
Autor:
Rodney H. White, Neil S. Isaacs, David J. Young, Stephen D. Hiscock, Rodney E. Sue, Malcolm D. King
Publikováno v:
The Journal of Organic Chemistry. 60:7166-7169
Allylic sulfinic acids have been prepared by cleavage of trialkyltin allylic sulfinates with trifluoroacetic acid (TFA). Allylsulfinic acid prepared in this way could be trapped as the sodium salt or observed by NMR and UV spectroscopy to undergo spo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39c808364adf5f3545c87429eab6329f
https://doi.org/10.1021/jo00127a022
https://doi.org/10.1021/jo00127a022
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 5:1869-1874
The p-hydroxyphenethyl halides 1(b-d) possess the minimum structural requirements for alkylating DNA with Ar-3′ participation and exhibit in vitro cytotoxicity and DNA alkylating ability/sequence selectivity which is diminished relative to more fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68f7bf57ecb548730891e4b10a74ad26
https://doi.org/10.1016/0960-894x(95)00310-p
https://doi.org/10.1016/0960-894x(95)00310-p
Publikováno v:
ChemInform. 25
The acidolysis of trialkyltin allylic sulfinates yields the corresponding sulfinic acids which undergo a first-order thermal decomposition with γ-syn substitution as predicted for a retro-ene mechanism.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09133a70b1a33c2e06224488683fcafb
https://doi.org/10.1002/chin.199419056
https://doi.org/10.1002/chin.199419056
Publikováno v:
ChemInform. 28
Allylic sulfonyl halides can be generated by halogenolysis of the corresponding triorganotin sulfinates. Allylic sulfonyl bromides and iodides undergo a first order, thermal desulfination with allylic rearrangement to yield the corresponding allylic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3cf15c01f4470184fcf15892ff06b1b
https://doi.org/10.1002/chin.199739063
https://doi.org/10.1002/chin.199739063
Autor:
Phuc Van Le, Fabienne Lacrampe, Justin Anthony Ripper, Ronald J. Quinn, George Nikolakopoulos, Rodney H. White, Ian D. Jenkins, Lilian Alcaraz, Priscila de Almeida Leone
Publikováno v:
The Journal of organic chemistry. 74(3)
Inspired by the novel spiro structures of a number of bioactive natural products such as the histrionicotoxins, a series of novel spiro scaffolds have been designed and robust syntheses developed. The scaffolds are ready-to-use building blocks and ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebc5a1b19b9851640c71da7b221cfd7d
https://pubmed.ncbi.nlm.nih.gov/19105637
https://pubmed.ncbi.nlm.nih.gov/19105637
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 5:2931
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::785923de9dc413647ec3282ee3cfd7d9
https://doi.org/10.1016/0960-894x(95)00504-m
https://doi.org/10.1016/0960-894x(95)00504-m
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :1797
The acidolysis of trialkyltin allylic sulfinates yields the corresponding sulfinic acids which undergo a first-order thermal decomposition with γ-syn substitution as predicted for a retro-ene mechanism.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c35b5e6771980c004b2732c314dad1e
https://doi.org/10.1039/c39930001797
https://doi.org/10.1039/c39930001797
Publikováno v:
ResearcherID
Allylic sulfonyl halides can be generated by halogenolysis of the corresponding triorganotin sulfinates. Allylic sulfonyl bromides and iodides undergo a first order, thermal desulfination with allylic rearrangement to yield the corresponding allylic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::118935d8a62846a9e48e8c43d9d99554
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:A1997XF71400047&KeyUID=WOS:A1997XF71400047
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:A1997XF71400047&KeyUID=WOS:A1997XF71400047
