Bifunctional chiral auxiliaries 4: Alkylation of enolates derived from 1,3-diacyl-trans-4,5-tetramethyleneimidazolidin-2-ones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. Stereochemical control and mechanistic aspects of the alkylation of [(η5-C5H5)Fe(L)(CO)(COCHR)]–Li+(L = PPh3, PPh2NEt2; R = Me, Et): X-ray crystal structure of [(η5-C6H5)Fe(PPh3)(CO){COCH(Me)Et}]
2. Asymmetric alkylation reactions of chiral imide enolates. A practical approach to the enantioselective synthesis of .alpha.-substituted carboxylic acid derivatives
3. Bifunctional chiral auxiliaries 1: the aldol reaction between dialkylboron enolates of 1,3-dipropionyl-trans-4,5-tetramethyleneimidazolidin-2-one and aldehydes
4. (+)-11,11′-Di-O-methylelaiophylidene – preparation from elaiophylin and total synthesis from (R)-3-hydroxybutyrate and (S)-malate
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1. Synthesis and stereoselective evaluation of a (1R)-(–)-myrtenal-derived pseudo C2-symmetric dodecaheterocycle as a potential heterofunctional chiral auxiliary;Tetrahedron Letters;2018-12
2. From determination of enantiopurity to the construction of complex molecules: The Horeau principle and its application in synthesis;Tetrahedron;2018-07
3. Formation of Nitriles, Carboxylic Acids, and Derivatives by Alkylation, Acylation, and Substitution;Comprehensive Organic Transformations;2018-02-28
4. Functionalized α-oximinoketones as building blocks for the construction of imidazoline-based potential chiral auxiliaries;Tetrahedron: Asymmetry;2015-02
5. Synthesis of ferrocene-containing six-membered cyclic ureas via α-ferrocenyl carbocations;RSC Advances;2015
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