Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Christopher J. Sinz"'
Autor:
Joseph Carpenter, Robert R. Knowles, Simon B. Blakey, Ian Mangion, Akio Kayano, Christopher J. Sinz, David W. C. MacMillan
Publikováno v:
Chem. Sci.. 2:308-311
A total synthesis of the marine natural product diazonamide A (1) has been accomplished. This work features a highly stereoselective synthesis of the C(10) quaternary center and the central furanoindoline core enabled by an iminium-catalyzed alkylati
Publikováno v:
Proceedings of the National Academy of Sciences. 101:5482-5487
Pyrroloindoline and bispyrroloindoline are a subclass of alkaloid structural motifs that commonly exhibit biological activity. An enantioselective organocatalytic approach to the synthesis of pyrroloindoline architecture is described. The addition–
Publikováno v:
Tetrahedron. 58:6561-6576
Herein we provide full details of studies which culminated in the first total synthesis of the polyene macrolide dermostatin A, confirming our earlier stereochemical assignment. A highly convergent synthesis was developed, featuring the cyanohydrin a
Publikováno v:
Angewandte Chemie International Edition. 40:3224-3227
An oxo-hexaene macrolide antibiotic, dermostatin A has been synthesized. Key features of the synthesis include the application of cyanohydrin acetonide couplings for the synthesis of the polyol portion, and the convergent introduction of the polyene
Publikováno v:
Tetrahedron Letters. 39:6811-6814
Lewis acids promote the coupling of 4-acetoxy-1,3-dioxanes 1 with crotyl-metal species to generate propionate motifs such as 2. The reactions show a marked dependence on Lewis acid, the crotyl metal species, and the presence and stereochemical dispos
Publikováno v:
ChemInform. 29
Lewis acids promote the coupling of 4-acetoxy-1,3-dioxanes 1 with crotyl-metal species to generate propionate motifs such as 2. The reactions show a marked dependence on Lewis acid, the crotyl metal species, and the presence and stereochemical dispos
Publikováno v:
ChemInform. 32
An oxo-hexaene macrolide antibiotic, dermostatin A has been synthesized. Key features of the synthesis include the application of cyanohydrin acetonide couplings for the synthesis of the polyol portion, and the convergent introduction of the polyene
Publikováno v:
ChemInform. 33
Publikováno v:
ChemInform. 33
Herein we provide full details of studies which culminated in the first total synthesis of the polyene macrolide dermostatin A, confirming our earlier stereochemical assignment. A highly convergent synthesis was developed, featuring the cyanohydrin a
The first direct enantioselective catalytic alpha-oxidation of carbonyls has been accomplished. The use of enamine catalysis has provided a new organocatalytic strategy for the enantioselective oxyamination of aldehydes, to generate alpha-oxyaldehyde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b7027d779e8aeff36444b9e635e9203
https://resolver.caltech.edu/CaltechAUTHORS:20170419-130607059
https://resolver.caltech.edu/CaltechAUTHORS:20170419-130607059