Sulfur Migration in Organic Synthesis
Author:
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/10426509908546427
Reference23 articles.
1. Organic synthesis using a migrating functional group: [1,2] and [1,3] phenylthio shifts in synthesis via allyl sulphides
2. A novel synthesis of α-sulfenylated aldehydes
3. Transformation of cyclic α-phenylthio aldehydes by stereoselective aldol reactions and phenylthio migration into spirocyclic lactones and ethers, and E-allylic alcohols with 1,4-related chiral centres
4. Acyclic stereoselection—13
5. Use of the E-vinyloxyborane derived from S-phenyl propanethioate for stereospecific aldol-type condensation. A simplified synthesis of the prelog-djerassi lactonic acid
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1. A Rh-catalyzed 1,2-sulfur migration/aza-Diels–Alder cascade initiated by aza-vinyl carbenoids from sulfur-tethered N-sulfonyl-1,2,3-triazoles;Chemical Communications;2015
2. Sulfur as a Bridge: Synthesis of Medium Rings via a Bicyclic Sulfonium Ion;Advanced Synthesis & Catalysis;2011-11
3. Sulfur-Participated Nazarov-Type Cyclization: A Simple and Efficient Synthesis for 3-Thio-1H-indenes;Advanced Synthesis & Catalysis;2009-06
4. Nucleophilic Substitution Reactions of 2‐Phenylthio‐Substituted Carbohydrate Acetals and Related Systems: Episulfonium Ions vs. Oxocarbenium Ions as Reactive Intermediates;European Journal of Organic Chemistry;2008-01-28
5. ChemInform Abstract: Sulfur Migration in Organic Synthesis;ChemInform;2001-01-16
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