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. Author manuscript; available in PMC: 2018 Dec 14.
Published in final edited form as: Chembiochem. 2017 Nov 9;18(24):2380–2384. doi: 10.1002/cbic.201700397

Table 2.

Activities and stereoselectivities of biocatalysts for the reaction of styrene with ethyl diazoacetate.a

graphic file with name nihms949502u1.jpg
catalyst yield [%] TTNb dr (cis:trans) ee cis [%]c ee trans [%]d
heme 16 80 13:87 0 −3
Ir(Me)-DPIX 40 200 29:71 −1 −4
BM3h-T268A/ heme 68 339 1:99 −11 −97
WIVS-FM*-T268A/C400G/Ir(Me)-DPIX 48 240 29:71 0 0
a

reaction conditions: 7.5 mM olefin, 10 mM EDA, 15 μM catalyst, in 0.1 M NaPI pH 6.0 100 mM NaCl buffer, 5-% DMF as cosolvent (reactions with heme and heme enzymes also contain 10 mM dithionite). TTN and stereoselectivities determined by chiral GC analysis.

b

TTN = total turnover number.

c

(1S, 2R) – (1R, 2S).

d

(1R, 2R) – (1S, 2S).