Total synthesis of a protected form of sphingofungin e using the [3,3]-sigmatropic rearrangement of an allylic thiocyanate as the key reaction

Carbohydrate Research

Volumn 345, Issue 17, 2010, Pages 2427-2437

  Martinková, Miroslava ^a   Gonda, Jozef ^a   Raschmanová, Jana Špaková ^a   Slaninková, Michaela ^a   Kuchár, Juraj ^a  

^a P J AFÁRIK UNIVERSITY   (Slovakia)

Author keywords

Aza Claisen rearrangement; Isothiocyanates; Sphingofungin E

Indexed keywords

AZA-CLAISEN REARRANGEMENT; CARBON ATOMS; COUPLING REACTION; D-GLUCOSE; FUNCTIONALIZED; HYDROPHOBIC SEGMENT; INTERCONVERSIONS; ISOTHIOCYANATES; KEY REACTIONS; SIGMATROPIC REARRANGEMENTS; SPHINGOFUNGIN E; STEREOCONTROLLED SYNTHESIS; TOTAL SYNTHESIS;

BROMINE COMPOUNDS; ETHERS; FUNCTIONAL GROUPS; GLUCOSE;

SYNTHESIS (CHEMICAL);

BROMIDE; FUNCTIONAL GROUP; GLUCOSE DERIVATIVE; NATURAL PRODUCT; SPHINGOFUNGIN E; THIOCYANATE; UNCLASSIFIED DRUG;

ARTICLE; CLAISEN REARRANGEMENT; CRYSTAL STRUCTURE; DRUG STRUCTURE; DRUG SYNTHESIS; PRIORITY JOURNAL; X RAY DIFFRACTION;

ALCOHOLS; AMINO ACIDS; AZA COMPOUNDS; FATTY ACIDS, UNSATURATED; GLUCOSE; THIOCYANATES;

EID: 78049296500     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carres.2010.09.016     Document Type: Article

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