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. Author manuscript; available in PMC: 2021 Aug 23.
Published in final edited form as: Nat Rev Chem. 2020 Jun 3;4:334–346. doi: 10.1038/s41570-020-0191-2

Figure 7 |. Engineering non-natural carbene transferases for biocatalytic C–C bond formation.

Figure 7 |

a | Natural iron-oxene formation in the haem cofactor of haemoproteins. b | Engineering artificial carbene-transferases through iron-carbene formation.151,168170 c | Scope of cyclopropanation reactions catalysed by carbene transferases158160,162164 and representative use in chemoenzymatic synthesis.166 d | Carbene transfer into alkyne forms highly strained cyclopropene and bicyclobutane products.165 e | Carbene insertion into C–H bonds forms alkylated products.168,169,171174 f | Carbene transferases have catalysed C–C bond formation through rearrangement reactions and Wittig reactions.175177