Attempted Methylenation of 1,2:3,4:5,6‐Tri‐O‐isopropylidene‐D‐gluconolactone Using Benzothiazol‐2‐ylmethylsulfone Under Julia Conditions Yields an Unusual Product
Author:
Affiliation:
1. a Department of Chemistry , Indian Institute of Technology Madras , Chennai
2. b Sophisticated Analytical Instrument Facility , Indian Institute of Technology Madras , Chennai
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/07328300701252417
Reference19 articles.
1. A Facile Synthesis of 1,2:3,4:5,6-Tri-O-Isopropylidene-D-Gluconate–A Convenient Precursor of the Open Chain form of D-Glucose
2. De Novo Synthesis of a Methylene-Bridged Neu5Ac-α-(2,3)-Gal C-Disaccharide
3. Synthesis of C-glycosyl compounds of N-acetylneuraminic acid from d-gluconolactone
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1. The Julia-Kocienski Olefination;Organic Reactions;2018-04-04
2. Mechanistic Manifold and New Developments of the Julia–Kocienski Reaction;European Journal of Organic Chemistry;2009-03-30
3. Attempted Methylenation of 1,2:3,4:5,6-Tri-O-isopropylidene-D-gluconolactone Using Benzothiazol-2-ylmethylsulfone under Julia Conditions Yields an Unusual Product (III).;ChemInform;2007-10-30
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