7115-22-2Relevant articles and documents
TOTAL SYNTHESIS OF (+)-CASTANOSPERMINE FROM D-MANNOSE
Setoi, Hiroyuki,Takeno, Hidekazu,Hashimoto, Masashi
, p. 4617 - 4620 (1985)
A total synthesis of (+)-castanospermine (2) has been achieved starting from D-mannose by a route adopting a double-cyclization process (5c-6) as the key step.
The synthesis of polyoxygenated, enantiomerically pure cyclopentane derivatives on route to neplanocin A stereoisomers via alkylidenecarbene species prepared from sugar templates
Nguyen Van Nhien, Albert,Soriano, Elena,Marco-Contelles, Jose,Postel, Denis
experimental part, p. 1605 - 1611 (2009/12/09)
Our new method for the generation of alkylidenecarbenes, based on the reaction of trimethylsilylazide/Bu2SnO with α-cyanomesylates, has been applied to the synthesis of enantiomerically pure polyhydroxylated cyclopentane derivatives from conven
The Baylis-Hillman reaction: a strategic tool for the synthesis of higher-carbon sugars
Radha Krishna, Palakodety,Narasimha Reddy,Sreeshailam,Uday Kiran,Jagdeesh
, p. 6466 - 6470 (2008/02/12)
The Baylis-Hillman reaction of acyclic sugar-derived aldehydes is invoked as an attractive synthetic strategy for ready access to higher-carbon sugars.