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pro vyhledávání: '"Jordan C. Beck"'
Publikováno v:
Chemical Science. 10:2315-2319
A modular synthesis of enantioenriched polyfunctionalized cyclobutanes was developed that features an 8-aminoquinolinamide directed C–H arylation reaction. The C–H arylation products were derivatized through subsequent decarboxylative coupling pr
Publikováno v:
ChemInform. 47
The first enantioselective total synthesis of the cytotoxic natural product (+)-psiguadial B is reported. Key features of the synthesis include (1) the enantioselective preparation of a key cyclobutane intermediate by a tandem Wolff rearrangement/asy
The first enantioselective total synthesis of the cytotoxic natural product (+)-psiguadial B is reported. Key features of the synthesis include (1) the enantioselective preparation of a key cyclobutane intermediate by a tandem Wolff rearrangement/asy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bee80351e7c8b22c3641cd11bfbabcb2
https://resolver.caltech.edu/CaltechAUTHORS:20160815-142455841
https://resolver.caltech.edu/CaltechAUTHORS:20160815-142455841