71021-15-3

Basic information

• Product Name: .beta.-D-erythro-Hex-2-enopyranose, 1,6-anhydro-2,3-dideoxy-, benzoate
• Synonyms: .beta.-D-erythro-Hex-2-enopyranose, 1,6-anhydro-2,3-dideoxy-, benzoate
• CAS NO: 71021-15-3
• Molecular Formula: C₁₃H₁₂O₄
• Molecular Weight: 232.24
• Mol File: 71021-15-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: .beta.-D-erythro-Hex-2-enopyranose, 1,6-anhydro-2,3-dideoxy-, benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: .beta.-D-erythro-Hex-2-enopyranose, 1,6-anhydro-2,3-dideoxy-, benzoate(71021-15-3)
• EPA Substance Registry System: .beta.-D-erythro-Hex-2-enopyranose, 1,6-anhydro-2,3-dideoxy-, benzoate(71021-15-3)

Safety Data

• Hazardous Substances Data: 71021-15-3(Hazardous Substances Data)

Upstream product

• 136573-60-9 1,5-anhydro-3,4-di-O-benzoyl-2-deoxy-D-arabino-hex-1-enitol 

Downstream Products

• 116429-46-0 Benzoic acid (1R,2S,3S,4R,5R)-3,4-dihydroxy-6,8-dioxa-bicyclo[3.2.1]oct-2-yl ester 
• 33647-85-7 isolevoglucosenone 
• 58394-31-3 1,6-anhydro-2,3-dideoxy-β-D-erythro-hex-2-enopyranose 

Relevant articles and documents

Clay montmorillonite in carbohydrates : Use of 'claysil' as an efficient heterogenous catalyst for the intramolecular Ferrier reactions leading to 1,6-anhydro rare saccharides

Clay montmorillonite supported silver reagent - claysil - was prepared and advantageously used in the intramolecular Ferrier reaction of 6-hydroxy glycals 1a-9c. The unsaturated sugars 13a-21c so obtained were stereoselectively hydroxylated leading to the

A ready method for generating oxycarbinyl radicals for conjugate-addition-alkylation or radical cyclization reactions

A ready method is described from generating oxycarbinyl radicals from alcohols, acetals and aldehydes which involves periodic addition of di-tert-butyl-hyponitrite (DBH) to a refluxing solution of the precursor.The resulting radicals may be trapped intermolecularly by α-enones in conjugate-addition-alkylation reactions, or intermolecularly in ring-forming reactions.Typically, small portions of DBH are added every 10-15 minutes until the reactant of interest has been consumed. Keywords: conjugate addition / carbohydrate α-enones / oxycarbinyl radicals

Synthesis of 1,6-anhydro-2,3-dideoxy-β-D-erythro- and -threo-hex-2-enopyranose from 3,4-di-O-substituted glycals by a facile intramolecular Ferrier reaction

The 1,6-anhydro-2,3-dideoxy-β-D-erythro- 7-9 and -threo-hex-2-enopyranoses 10-12 are valuable synthons for the preparation of structurally diverse natural products. This paper reports on a new, general, and efficient route to their synthesis from 3,4-di-O