1995
DOI: 10.1002/aoc.590090313
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Reagent control of stereochemistry in allylic additions to chiral aldehydes with CpMo(NO)(X)(2‐methallyl) complexes of high enantiomeric purity

Abstract: Reactions of (R)-and (S)-CpMo(NO)(q3-methallyl

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Cited by 6 publications
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“…The precursors for oxygen heterocycle formation—the racemic or enantiopure enallenols 1 a and 1 b (Scheme , below) and 1 c and 1 d (Scheme , below)—were readily prepared from the appropriate starting 4‐oxoazetidine‐2‐carbaldehydes through regiocontrolled indium‐mediated Barbier‐type carbonyl–allenylation reactions in aqueous media, as we have previously described 10a. The optically active precursors syn ‐ 1 e and anti ‐ 1 e were prepared from homomethallylic alcohol 2 and aldehyde 3 10b in a four‐step sequence as shown in Scheme . Enallenol 1 f was prepared from salicylaldehyde by using our methodology 10c…”
Section: Resultsmentioning
confidence: 99%
“…The precursors for oxygen heterocycle formation—the racemic or enantiopure enallenols 1 a and 1 b (Scheme , below) and 1 c and 1 d (Scheme , below)—were readily prepared from the appropriate starting 4‐oxoazetidine‐2‐carbaldehydes through regiocontrolled indium‐mediated Barbier‐type carbonyl–allenylation reactions in aqueous media, as we have previously described 10a. The optically active precursors syn ‐ 1 e and anti ‐ 1 e were prepared from homomethallylic alcohol 2 and aldehyde 3 10b in a four‐step sequence as shown in Scheme . Enallenol 1 f was prepared from salicylaldehyde by using our methodology 10c…”
Section: Resultsmentioning
confidence: 99%