Kinetic and thermodynamic azides from α-triflates of γ-lactones: intermediates for the incorporation of polyhydroxylatedD- andL-α-aminoacids into combinatorial libraries-Reference-Cited by-同舟云学术

Kinetic and thermodynamic azides from α-triflates of γ-lactones: intermediates for the incorporation of polyhydroxylatedD- andL-α-aminoacids into combinatorial libraries

Published:1996 Issue:11 Volume: Page:1271-1272
ISSN:1359-7345
Container-title:Chem. Commun.
language:en
Short-container-title:Chem. Commun.

Author:

Krülle Thomas M.,Davis Benjamin,Ardron Helen,Long Daniel D.,Hindle Neil A.,Smith Colin,Brown David,Lane Alexandra L.,Watkin David J.,Marquess Daniel G.,Fleet George W. J.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/1996/CC/CC9960001271

Reference16 articles.

1. Deoxyiminoalditols from Aldonolactones; IV: Preparation of 1,5-Dideoxy-1,5-iminoheptitols with L-glycero-D-manno, D-glycero-L-gulo and L-glycero-D-altro Configuration

2. Selectively tosylated aldonolactones as precursors for highly functionalized, enantiomerically pure tetrahydrofurans

3. Acetonides of octonolactones

4. The synthesis of polyhydroxylated amino acids from glucuronolactone: enantiospecific syntheses of 2s, 3r, 4r, 5s-trihydroxypipecolic acid, 2r, 3r, 4r, 5s-trihydroxypipecolic acid and 2r, 3r, 4r-dihydroxyproline

5. Synthesis of 2s, 4s, 5s -dihydroxypipecolic acid and bulgecinine [2s,4s,5r-4-hydroxy-5- (hydroxymethyl)proline] from d-glucuronolactone, a strategy for the synthesis of 2s,4s-4-hydroxy-α-amino acids

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