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000896719 1001_ $$0P:(DE-Juel1)166432$$aMantel, Marvin$$b0
000896719 245__ $$aLewis Base–Brønsted Acid–Enzyme Catalysis in Enantioselective Multistep One‐Pot Syntheses
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000896719 520__ $$aEstablishing one-pot, multi-step protocols combining different types of catalysts is one important goal for increasing efficiency in modern organic synthesis. In particular, the high potential of biocatalysts still needs to be harvested. Based on an in-depth mechanistic investigation of a new organocatalytic protocol employing two catalysts {1,4-diazabicyclo[2.2.2]octane (DABCO); benzoic acid (BzOH)}, a sequence was established providing starting materials for enzymatic refinement (ene reductase; alcohol dehydrogenase): A gram-scale access to a variety of enantiopure key building blocks for natural product syntheses was enabled utilizing up to six catalytic steps within the same reaction vessel.
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000896719 7001_ $$0P:(DE-HGF)0$$aGiesler, Markus$$b1
000896719 7001_ $$0P:(DE-Juel1)159507$$aGuder, Marian$$b2
000896719 7001_ $$0P:(DE-Juel1)145645$$aRüthlein, Elisabeth$$b3
000896719 7001_ $$0P:(DE-HGF)0$$aHartmann, Laura$$b4
000896719 7001_ $$0P:(DE-Juel1)128906$$aPietruszka, Jörg$$b5$$eCorresponding author
000896719 773__ $$0PERI:(DE-600)2011836-3$$a10.1002/anie.202103406$$gVol. 60, no. 30, p. 16700 - 16706$$n30$$p16700 - 16706$$tAngewandte Chemie / International edition$$v60$$x1521-3773$$y2021
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