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pro vyhledávání: '"Henry C. Hsu"'
Autor:
Henry C. Hsu
Publikováno v:
The Journal of the Acoustical Society of America. 88:591-591
A slat for use in the assembly of a Venetian blind is provided with a light and sound absorptive coating on at least one of its major surfaces produced by flocking, applique, or textile weaving techniques, a preferred embodiment of the invention prov
Publikováno v:
Synthetic Communications. 11:247-251
Vinyl halides are important synthetic intermediates. One route to vinyl halides involves the reaction of vinylboronic acids with halogens in the presence of sodium hydroxide. Although the reaction of iodine with organoborane reagents has been careful
Publikováno v:
The Journal of Organic Chemistry. 52:827-836
We present a new synthetic strategy for preparing tetraphenylporphyrins that should greatly expand synthetic entries into porphyrin containing model systems. Pyrrole and the desired benzaldehyde react reversibly at room temperature with trace acid ca
Publikováno v:
The Journal of Organic Chemistry. 46:3113-3115
Autor:
Henry C. Hsu, Raymond L. Hayes, E. Eugene Gooch, George W. Kabalka, Tan Tan Sun, Lee C. Washburn
Radioiodinated estrogen derivatives of potential use as receptor-binding agents have been synthesized via the reaction of organoboranes with 125 ICl, The utility of organoboranes as intermediates in radiopharmaceutical syntheses is discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acb8d680f70daab29ca00f80896493af
https://doi.org/10.1016/b978-0-08-027544-4.50023-x
https://doi.org/10.1016/b978-0-08-027544-4.50023-x
Publikováno v:
ChemInform. 18
We present a new synthetic strategy for preparing tetraphenylporphyrins that should greatly expand synthetic entries into porphyrin containing model systems. Pyrrole and the desired benzaldehyde react reversibly at room temperature with trace acid ca
Publikováno v:
ChemInform. 18
Reaction of pyrrole and an aromatic aldehyde at room temperature affords the corresponding tetraarylporphyrinogen in high yield at thermodynamic equilibrium. Oxidation yields the porphyrin. The reaction conditions are of broad scope.
Publikováno v:
Tetrahedron Letters. 27:4969-4970
Reaction of pyrrole and an aromatic aldehyde at room temperature affords the corresponding tetraarylporphyrinogen in high yield at thermodynamic equilibrium. Oxidation yields the porphyrin. The reaction conditions are of broad scope.