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THE RING CONTRACTION OF DELTA-...
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THE RING CONTRACTION OF DELTA-LACTONES WITH LEAVING GROUP ALPHA-SUBSTITUENTS - A STRATEGY FOR THE SYNTHESIS OF 2,5-DISUBSTITUTED HIGHLY FUNCTIONALIZED HOMOCHIRAL TETRAHYDROFURANS
Dades bibliogràfiques
Autors principals:
Choi, S
,
Myerscough, P
,
Fairbanks, A
,
Skead, B
,
Bichard, C
,
Mantell, S
,
Son, J
,
Fleet, G
,
Saunders, J
,
Brown, D
Format:
Journal article
Idioma:
English
Publicat:
1992
Fons
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ACID-CATALYZED TRANSFORMATION OF ALPHA-TRIFLUOROMETHANESULFONATES OF GAMMA-LACTONES AND DELTA-LACTONES INTO 2,5-DISUBSTITUTED HOMOCHIRAL TETRAHYDROFURANS
per: Wheatley, J, et al.
Publicat: (1993)
CYCLIC SULFATES OF DELTA-LACTONES IN THE SYNTHESIS OF TETRAHYDROFURANS TETRAHYDROPYRANS AND CYCLOHEXANES
per: Skead, B, et al.
Publicat: (1993)
Branched tetrahydrofuran alpha,alpha-disubstituted-delta-sugar amino acid scaffolds from branched sugar lactones: a new family of foldamers?
per: Simone, M, et al.
Publicat: (2005)
Complex tetrahydrofurans from carbohydrate lactones: Easy access to epimeric C-glycosides of glucofuranose from D-glycero-D-gulo-heptono-1,4-lactone
per: Bichard, C, et al.
Publicat: (1996)
Templated scaffolds of cis- and trans-tetrahydrofuran gamma-amino acids: gamma-azido-beta-hydroxy-tetrahydrofuran-2-carboxylates from pentono-delta-lactones
per: Sanjayan, G, et al.
Publicat: (2003)