Stereoselective Chemo-Enzymatic Approaches to the Synthesis of C 2 1,3-Dithiane-1,3-dioxide
Author:
Affiliation:
1. a Istituto di Chimica Organica “A. Marchesini” , Milano, Italy
2. b Dipartimento di Chimica Organica e Industriale , Milano, Italy
3. c Istituto di Chimica del Riconoscimento Molecolare–CNR , Milano, Italy
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10426500902856446
Reference16 articles.
1. Additions of aldehydes to metallated trans-1,3-Dithiane-S,S-dioxide under conditions of kinetic and thermodynamic control
2. Highly stereoselective addition reactions of metallated trans-1,3-dithiane-1,3-dioxide to aldehydes
3. Anion Reactions of 1,3-Dithiane 1,3-Dioxide with Carbonyl Compounds: High Diastereoselectivity with Aromatic Aldehydes under Conditions of Equilibrium Control
4. trans-1,3-Dithiane-1,3-dioxide, a new chiral acyl anion equivalent for the preparation of masked activated acids: application to the synthesis of α-hydroxy acid derivatives
5. trans-1,3-dithiane-1,3-dioxide; a chiral acyl anion equivalent. Enantioselective synthesis of α-hydroxy- carboxylic acids, esters, amides and ketones
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