1999
DOI: 10.1016/s0040-4020(99)00596-7
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On the possibility of carbamate-directed hydroboration. An approach to the asymmetric synthesis of 1-aminocyclopentane-1,3-dicarboxylic acid

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Cited by 22 publications
(15 citation statements)
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“…In a similar way, (1 S ,3 R )- 256 was transformed into (1 S ,3 S )-ACPD 506 in 34% overall yield (Scheme 104). 207…”
Section: Synthesis Of 1-aminocycloalkanecarboxylic Acidsmentioning
confidence: 99%
“…In a similar way, (1 S ,3 R )- 256 was transformed into (1 S ,3 S )-ACPD 506 in 34% overall yield (Scheme 104). 207…”
Section: Synthesis Of 1-aminocycloalkanecarboxylic Acidsmentioning
confidence: 99%
“…A series of phenethylamines, important substructures in biologically relevant molecules such as dopamine, amphetamine, and adrenaline, have recently been prepared by the hydroboration of enamines using 9-BBN [39]. Although the amine-directed uncatalyzed hydroboration using H 3 BÁTHF is known [40,41], to the best of our knowledge, the metal catalyzed hydroboration of enamines has not yet been reported. While a number of different transition metals are known to catalyze hydroborations, reactions employing rhodium complexes are the most common.…”
Section: Resultsmentioning
confidence: 99%
“…N-Boc-β-aminoketones 3a, 3b, 3c, 3d, 3e and 3g are new compounds while 3f is a known compound. 23 Characterization data are reported in the Electronic Supplementary Information (ESI).…”
Section: Methodsmentioning
confidence: 99%