Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Pachter, Irwin J."'
Autor:
Woodward, R. B., Pachter, Irwin J.
Publikováno v:
ETSU Faculty Works.
Reliable procedures for the preparation of trimethylene and ethylene dithiotosylates are reported. Techniques for the formation of dithianes and dithiolanes by reaction of these reagents with activated methylene groups are described; these include pr
Externí odkaz:
https://dc.etsu.edu/etsu-works/12033
Autor:
Pachter, Irwin J.
Publikováno v:
Science, 1973 Jan . 179(4070), 230-230.
Externí odkaz:
https://www.jstor.org/stable/1735657
Publikováno v:
Toxicologic Pathology; Feb1985, Vol. 13 Issue 2, p141-146, 6p
Autor:
Monkovic, Ivo, Wong, Henry, Pircio, Anthony W., Perron, Yvon G., Pachter, Irwin J., Belleau, Bernard
Publikováno v:
Canadian Journal of Chemistry; 1975, Vol. 53 Issue 20, p3094-3102, 9p
Publikováno v:
Canadian Journal of Chemistry; 1975, Vol. 53 Issue 17, p2515-2523, 9p
Autor:
Girard H. Hottendorf, Pachter Irwin J
Publikováno v:
Toxicologic Pathology. 13:141-146
A comparison of the carcinogenesis bioassay results obtained by the National Cancer Institute (NCI) and the National Toxicology Program (NTP) indicates that approximately one-half of the bioassays directed by both institutions were positive for carci
Autor:
Bernard Belleau, Henry Wong, Anthony W. Pircio, Yvon G. Perron, Pachter Irwin J, Ivo Monkovic
Publikováno v:
Canadian Journal of Chemistry. 53:3094-3102
A series of 3,14-dihydroxymorphinans 8 was synthesized via a method of (a) acylation of 3-methoxy-Δ8,14-morphinan 4a (b) stereospecific epoxidation of the resultant amides to β-epoxides 5 (c) simultaneous reduction of amide and epoxide functions an
Autor:
G. H. Hottendorf Dvm, Pachter Irwin J
Publikováno v:
Toxicologic Pathology. 10:22-26
Tabulations of the results of the initial approximately 200 NCI carcinogenesis bioassays conducted in mice and rats were published recently. However, no analysis of the results were provided. Such an analysis is the subject of this report. Ninety eig
Publikováno v:
Canadian Journal of Chemistry. 53:2515-2523
The synthesis of a versatile intermediate 4a-(2-aminoethyl)-l,2,3,4,4a,9-hexahydro-6-methoxyphenanthrene (3a) and its utilization in the synthesis of 9α-hydroxy-3-methoxy-17-methylhasubanan (10), 3,14-dimethoxy-17-methylisomorphinan (9l), various 14
Publikováno v:
Canadian Journal of Chemistry; September 1975, Vol. 53 Issue: 17 p2515-2523, 9p