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. Author manuscript; available in PMC: 2011 Oct 12.
Published in final edited form as: Org Lett. 2009 Feb 19;11(4):943–946. doi: 10.1021/ol802930q

Table 2.

Scope of HNR1R2 in enantioselective synthesis of (S)-β-fluoroamines.

graphic file with name nihms91352t2.jpg

compda product yield (%)b ee (%)c
7a graphic file with name nihms91352t3.jpg 80 >99 (S)
7b graphic file with name nihms91352t4.jpg 70 >98 (S)
7c graphic file with name nihms91352t5.jpg 76 >99 (S)
7d graphic file with name nihms91352t6.jpg 69 >98 (S)
7e graphic file with name nihms91352t7.jpg 65 >96 (S)
7f graphic file with name nihms91352t8.jpg 82 >95 (S)
a

All reactions were performed on a 0.5 mmol scale and proceeded to complete conversion.

b

Yield after chromatography.

c

Enantiomeric excess were determined using chiral stationary phase