Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Justin T. J. Spence"'
Autor:
Andrei S. Baluna, Albano Galan, David A. Leigh, Gareth D. Smith, Justin T. J. Spence, Daniel J. Tetlow, Iñigo J. Vitorica-Yrezabal, Min Zhang
Publikováno v:
Journal of the American Chemical Society. 145:9825-9833
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c607907da865aa813e0fbcb6f8f1edd
https://doi.org/10.1021/jacs.3c01939
https://doi.org/10.1021/jacs.3c01939
Autor:
Chong Tian, Daniel J. Tetlow, Malcolm A. Y. Gall, Javier Echavarren, Justin T J Spence, David A. Leigh, Adrian Haertsch
Publikováno v:
Journal of the American Chemical Society
We report on the preparation of a decapeptide through the parallel operation of two rotaxane-based molecular machines. The synthesis proceeds in four stages: (1) simultaneous operation of two molecular peptide synthesizers in the same reaction vessel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f04960f64593b6301e7fbaa4e0b3bf47
https://doi.org/10.1021/jacs.1c01234
https://doi.org/10.1021/jacs.1c01234
Publikováno v:
Angewandte Chemie (International ed. in English). 55(35)
Hyperjapones A-E and hyperjaponols A-C are complex natural products of mixed aromatic polyketide and terpene biosynthetic origin that have recently been isolated from Hypericum japonicum. We have synthesized hyperjapones A-E using a biomimetic, oxida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cf7ee26ce3612ab21cce908003db63f
https://pubmed.ncbi.nlm.nih.gov/27461748
https://pubmed.ncbi.nlm.nih.gov/27461748
Publikováno v:
Organic letters. 17(24)
The total synthesis of peniphenones A-D has been achieved via Michael reactions between appropriate nucleophiles and a common o-quinone methide intermediate. This strategy, which was based on a biosynthetic hypothesis, minimized the use of protecting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bee5aeb4f39629c6b537e0cf1430946
https://pubmed.ncbi.nlm.nih.gov/26634635
https://pubmed.ncbi.nlm.nih.gov/26634635
Publikováno v:
Organic Letters. 13:5318-5321
A structure revision for the recently isolated fungal meroterpenoids, cytosporolides A-C, is suggested based on biosynthetic speculation and reinterpretation of existing spectroscopic data. The structure revision is supported by a biomimetic syntheti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::557627ed6777001022fdad649417a526
https://doi.org/10.1021/ol202181g
https://doi.org/10.1021/ol202181g
Publikováno v:
Organicbiomolecular chemistry. 12(15)
Protected cyclohexanol and cyclohex-2-enol substrates, containing benzyl ether and benzoate ester moieties, were designed to fit into the active site of the Tyr96Ala mutant of cytochrome P450cam. The protected cyclohexanol substrates were efficiently
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65e5248fc69c2d026ec5d368ed28ccd3
https://pubmed.ncbi.nlm.nih.gov/24599100
https://pubmed.ncbi.nlm.nih.gov/24599100
Publikováno v:
Organic letters. 15(15)
The total synthesis of ent-penilactone A and penilactone B has been achieved via biomimetic Michael reactions between tetronic acids and o-quinone methides. A five-component cascade reaction between a tetronic acid, formaldehyde, and a resorcinol der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0f6e6f6e58a8edf933174958fa6764f
https://pubmed.ncbi.nlm.nih.gov/23837511
https://pubmed.ncbi.nlm.nih.gov/23837511
Publikováno v:
Organic Letters; Oct2011, Vol. 13 Issue 19, p5318-5321, 4p