Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Julius R. Reyes"'
Publikováno v:
Organic Syntheses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38deff2553ea4284e1f432fb2403d9a1
https://doi.org/10.1002/0471264229.os096.05
https://doi.org/10.1002/0471264229.os096.05
Publikováno v:
Angewandte Chemie. 130:15813-15817
The cytochalasans are a large family of polyketide natural products with potent bioactivities. Amongst them, the aspochalasins show particularly intricate and fascinating structures. To gain insight into their structural diversity and innate reactivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3905550a77606f65e3f4910866aab86c
https://doi.org/10.1002/ange.201809703
https://doi.org/10.1002/ange.201809703
Publikováno v:
Angewandte Chemie International Edition. 56:9962-9966
The asymmetric synthesis of (−)-N-methylwelwitindolinone B isothiocyanate is reported. Critical challenges overcome through these studies include the stereoselective installation of the sterically congested C13 alkyl chloride and control of the way
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5cc35715570a80573dd556f10c2315b
https://doi.org/10.1002/anie.201705322
https://doi.org/10.1002/anie.201705322
Autor:
Julius R. Reyes, Bichu Cheng
Publikováno v:
Natural product reports. 37(3)
Covering: 2006 to 2019Macrocyclic diamine alkaloids derived from 3-alkyldihydropyridine dimers comprise a diverse and highly complex family of natural products. The macrocyclic and caged structural features of these alkaloids have inspired many creat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ac49d0a02a8240de25a99acf0c8d79c
https://pubmed.ncbi.nlm.nih.gov/31524907
https://pubmed.ncbi.nlm.nih.gov/31524907
Autor:
Julius R. Reyes, Viresh H. Rawal
Publikováno v:
Angew Chem Int Ed Engl
A method is presented for the direct transformation of a ketone to the corresponding reduced alkyl chloride or bromide. The process involves the reaction of a ketone trityl hydrazone with tBuOCl to give a diazene which readily collapses to the α-chl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::312d54d1882a4235ea451520d6e43763
https://doi.org/10.1002/ange.201510909
https://doi.org/10.1002/ange.201510909
Autor:
Julius R. Reyes, Dirk Trauner
Publikováno v:
Synfacts. 2019:0558
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ca8858978a705d1ea93c5d099c6c1e7
https://doi.org/10.1055/s-0037-1612499
https://doi.org/10.1055/s-0037-1612499
Autor:
Dirk Trauner, Julius R. Reyes
Publikováno v:
Synfacts. 2019:0560
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8384c1f2ef77ef321859024cc71d122
https://doi.org/10.1055/s-0037-1612500
https://doi.org/10.1055/s-0037-1612500
Autor:
Dirk Trauner, Julius R. Reyes
Publikováno v:
Synfacts. 15:0436
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a880d2ff57aeef792ca5968564fd9f8d
https://doi.org/10.1055/s-0037-1612405
https://doi.org/10.1055/s-0037-1612405
Autor:
Dirk Trauner, Julius R. Reyes
Publikováno v:
Synfacts. 15:0439
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14e85a8742d4ccaa832dd6c685744642
https://doi.org/10.1055/s-0037-1612404
https://doi.org/10.1055/s-0037-1612404
Autor:
Dirk Trauner, Julius R. Reyes
Publikováno v:
Synfacts. 15:0440
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::014ad9a779950c873f5b5d9a16a19dc5
https://doi.org/10.1055/s-0037-1612406
https://doi.org/10.1055/s-0037-1612406