Zobrazeno 1 - 6
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pro vyhledávání: '"Jennifer M. Goss"'
Publikováno v:
ChemInform. 42
Chiral organic Bronsted bases have emerged as highly efficient catalysts for enantioselective transformations. Since their early use in enantiomeric separation processes, chiral organic Bronsted base catalysis has advanced significantly to include bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b31c35b71c3db31ac02652604148446
https://doi.org/10.1002/chin.201123230
https://doi.org/10.1002/chin.201123230
Publikováno v:
Topics in current chemistry. 291
Chiral organic Brønsted bases have emerged as highly efficient catalysts for enantioselective transformations. Since their early use in enantiomeric separation processes, chiral organic Brønsted base catalysis has advanced significantly to include
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::baa4c20e66c9b39035e3e74ee4bc53ff
https://pubmed.ncbi.nlm.nih.gov/21494951
https://pubmed.ncbi.nlm.nih.gov/21494951
Autor:
Jonathan C. Schroeder, Jean-Philippe Fortin, Scott E. Schaus, Jennifer M. Goss, Carmit Goldstein, Alan S. Kopin, Martin Beinborn
The melanin-concentrating hormone (MCH) receptor type 1 (MCHR1) is a seven-transmembrane domain protein that modulates orexigenic activity of MCH, the corresponding endogenous peptide agonist. MCH antagonists are being explored as a potential treatme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d30f0ddc9505566f1c379a9ada28264
https://europepmc.org/articles/PMC2993548/
https://europepmc.org/articles/PMC2993548/
Publikováno v:
Organic Syntheses
Carbamic acid, 2-propen--1-yl ester Carbamic acid, N-[phenyl(phenylsulfonyl)methyl]-,2-propen-1-yl ester (betaR)-Benzenpropanoic acid, alpha acetyl-beta-[[(2-propen-1-yloxy)carbonyl]amino]-methyl ester (betaR)-Benzenepropanoic acid, alpha acetyl-beta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0109a2eebdf195cc80e93836ce8f061
https://doi.org/10.1002/0471264229.os086.23
https://doi.org/10.1002/0471264229.os086.23
Publikováno v:
Topics in Current Chemistry ISBN: 9783642028144
Chiral organic Bronsted bases have emerged as highly efficient catalysts for enantioselective transformations. Since their early use in enantiomeric separation processes, chiral organic Bronsted base catalysis has advanced significantly to include bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c874cef85fae9c3bb1db0054ec007d4
https://doi.org/10.1007/978-3-642-02815-1_23
https://doi.org/10.1007/978-3-642-02815-1_23
Autor:
Scott E. Schaus, Jennifer M. Goss
Publikováno v:
ChemInform. 40
An enantioselective synthesis of SNAP-7941, a potent melanin concentrating hormone receptor antagonist, was achieved by using two organocatalytic methods. The first method utilized to synthesize the enantioenriched dihydropyrimidone core was the Cinc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b8d6425b5bb79478676f5e373e8eaad
https://doi.org/10.1002/chin.200907172
https://doi.org/10.1002/chin.200907172