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1226589-78-1

(1R,2R)-2-methylcyclopropane-1-carbaldehyde synthesis

6synthesis methods
2-Butenal, 4-bromo-3-methyl-, (E)- (9CI)

31930-41-3
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Cyclopropanecarboxaldehyde, 2-methyl-, (1S,2S)-

394735-00-3
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(1R,2R)-2-methylcyclopropane-1-carbaldehyde

1226589-78-1
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(1S,2R)-2-methylcyclopropane-1-carbaldehyde

397266-17-0
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Yield:22 % ee

Reaction Conditions:

with wild-type 12-oxophytodienoicacid reductase 3 from Solanum lycopersicum Y190F mutant;NADH in aq. phosphate buffer;N,N-dimethyl-formamide at 25; pH=7.5; for 3 h;Darkness;Inert atmosphere;Schlenk technique;Enzymatic reaction;Reagent/catalyst;

References:

Heckenbichler, Kathrin;Schweiger, Anna;Brandner, Lea Alexandra;Binter, Alexandra;Toplak, Marina;Macheroux, Peter;Gruber, Karl;Breinbauer, Rolf [Angewandte Chemie - International Edition,2018,vol. 57,# 24,p. 7240 - 7244][Angew. Chem.,2018,# 130,p. 7360 - 7364,5] Location in patent:supporting information

152518-89-3 Synthesis
[(1R,2R)-2-METHYLCYCLOPROPYL]METHANOL

152518-89-3
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(1R,2R)-2-methylcyclopropane-1-carbaldehyde

1226589-78-1
1 suppliers
inquiry