Use of methanesulfonic acid in the reductive ring-opening of O-benzylidene acetals

Carbohydrate Research

Volumn 342, Issue 3-4, 2007, Pages 627-630

  Zinin, Alexander I ^a   Malysheva, Nelly N ^a   Shpirt, Anna M ^a   Torgov, Vladimir I ^a   Kononov, Leonid O ^a  

^a N D ZELINSKY INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

Author keywords

Benzylidene acetal; Methanesulfonic acid; Reduction; Regioselectivity; Sodium cyanoborohydride

Indexed keywords

BENZYLIDENE ACETAL; METHANESULFONIC ACID; REGIOSELECTIVITY; SODIUM CYANOBOROHYDRIDE;

ETHERS; HYDROCHLORIC ACID; ORGANIC ACIDS; REACTION KINETICS; REDUCTION; STEREOCHEMISTRY;

ACETAL RESINS;

4,6 BENZYLIDENE; ACETAL DERIVATIVE; BENZYLIDENE DERIVATIVE; CHLORIDE; CYANOBOROHYDRIDE SODIUM; HYDROXIDE; MESYLIC ACID; SODIUM BOROHYDRIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; PRIORITY JOURNAL; RING OPENING; SYNTHESIS;

ACETALS; BENZYLIDENE COMPOUNDS; BOROHYDRIDES; MESYLATES; OXIDATION-REDUCTION;

EID: 33846482568     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2006.10.009     Document Type: Article

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