Zobrazeno 1 - 10 of 114 pro vyhledávání: '"Walter J. Gensler"'
1
The Synthesis of Isoquinolines by the Pomeranz-Fritsch Reaction
Autor: Walter J. Gensler
Publikováno v: Organic Reactions
Acid-catalyzed cyclization of benzalaminoacetal results in the formation of the isoquinoline nucleus. This reaction, first reported by Pomeranz and Fritsch, has been used in the synthesis of a variety of isoquinoline compounds. The process is carried
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::eebcbe196d3e36c8e06198f396e55f89
https://doi.org/10.1002/0471264180.or006.04
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3
Nonenolizable podophyllotoxin derivatives
Autor: Walter J. Gensler, Marion H. Trammell, C. D. Murthy
Publikováno v: Journal of Medicinal Chemistry. 20:635-644
To block epimerization and the resulting biological deactivation podophyllotoxin compounds, the lactone carbonyl group has been changed to methylene. Syntheses of several of these delactonized derivatives are described, all with modifications in the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3802553b0b3731334c34a30021e2fd4f
https://doi.org/10.1021/jm00215a004
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5
3-Hydroxy-2-alkyl carboxylic acids related to mycolic acid
Autor: Walter J. Gensler, Iftekhar Alam, A.P. Chaudhuri, A.I. Radhakrishna, R. S. Prasad
Publikováno v: Tetrahedron. 35:2595-2600
A series of long-chain 3-hydroxy-2-alkyl acids structurally analogous to mycolic acids are reported. The synthesis applied, making use of 3-keto esters as intermediates, permits the insertion of 2-alkyl groups having no structural relationship to the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fdf2e3ce14f67c09d788b4c28bb26a63
https://doi.org/10.1016/0040-4020(79)88026-6
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