Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Alan Dinner"'
Publikováno v:
Journal of drugs in dermatology : JDD. 13(3)
Limonia acidissima or Hesperethusa crenulata is a common tree in Southeast Asia. It is indigenous to the Republic of Myanmar (formerly Burma) as well as India, Sri Lanka, Java, and Pakistan. In English, the common names for Limonia acidissima are san
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::073a3296a74d59967e6ae570493251d5
https://pubmed.ncbi.nlm.nih.gov/24595576
https://pubmed.ncbi.nlm.nih.gov/24595576
Autor:
Alan Dinner, John Fose
Publikováno v:
Drug Information Journal. 23:501-509
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3c775ebca87e9bfdf164d3840612e1e
https://doi.org/10.1177/009286158902300327
https://doi.org/10.1177/009286158902300327
Publikováno v:
Journal of Heterocyclic Chemistry. 5:191-194
A total of seven thiophene derivatives not previously reported have been prepared via the Knoevenagel condensation of an activated methylthiophene and a heterocyclic or aromatic aldehyde. The principal peaks in the ultraviolet and visible absorption
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::def800737c14c4f3e8a7063e632461cb
https://doi.org/10.1002/jhet.5570050206
https://doi.org/10.1002/jhet.5570050206
Publikováno v:
Journal of Heterocyclic Chemistry. 8:755-758
A variety of eleclrophilic substitution reactions have been carried out on 4-methoxybenzo[b]-thiophene (IIIa) and 4-benzoyloxybenzo[b ] thiophene (IVa). Substitution occurs in the 7-position of IIIa and, with the exception of bromination, in the 7-po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d223d9666962969fca7cdde77eb4e465
https://doi.org/10.1002/jhet.5570080514
https://doi.org/10.1002/jhet.5570080514
Autor:
Rex W. Souter, Alan Dinner
Publikováno v:
Journal of Pharmaceutical Sciences. 65:457-459
A convenient GLC method was developed to assay the chemically related CNS agents dl ‐3‐( p ‐trifluoromethylphenoxy)‐ N ‐methyl‐3‐phenylpropylamine (Ia) and dl ‐3‐( o ‐methoxy‐phenoxy)‐ N ‐methyl‐3‐phenylpropylamine (Ib).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b4c87cab70f65623790d6a856c0b0f7
https://doi.org/10.1002/jps.2600650341
https://doi.org/10.1002/jps.2600650341
Publikováno v:
The Journal of Organic Chemistry. 37:3539-3541
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35f6eacc70c1db6d4f7aa2658fff611c
https://doi.org/10.1021/jo00795a033
https://doi.org/10.1021/jo00795a033
Publikováno v:
Journal of Heterocyclic Chemistry. 7:695-697
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::805926fa1c382a4d7e9647845065b6b7
https://doi.org/10.1002/jhet.5570070339
https://doi.org/10.1002/jhet.5570070339
Publikováno v:
Journal of pharmaceutical sciences. 64(7)
A rapid, sensitive, and accurate GLC method of analysis of a new estrogenic drug, 17 alpha-ethynylestriol 3-cyclopentyl ether, was developed. The drug and the internal standard, tetratriacontane, are dissolved in chloroform, and an aliquot is heated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf7578c86b6354b6ebfd2ad15210e46e
https://pubmed.ncbi.nlm.nih.gov/1151685
https://pubmed.ncbi.nlm.nih.gov/1151685
Publikováno v:
Journal of medicinal chemistry. 18(3)
The preparation, characterization, and estrogenic activity of the two new steroids 3-(cylopentyloxy)-2',3'-dihydroestra-1,3,5(10)-trieno(16alpha,17alpha-b)furan-17beta-ol and 2',3'-dihydroestra-1,3,5(10)-trieno(16alpha,17alphs-b)furan-3,17beta-diol a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::091fe4631cdbe85f5796da4a51968604
https://pubmed.ncbi.nlm.nih.gov/1133824
https://pubmed.ncbi.nlm.nih.gov/1133824
Autor:
Alan Dinner, E. Campaigne
Publikováno v:
Journal of medicinal chemistry. 13(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f900c4073de6682a8a8946aa397f253f
https://pubmed.ncbi.nlm.nih.gov/5312307
https://pubmed.ncbi.nlm.nih.gov/5312307