86117-81-9Relevant academic research and scientific papers
Chemoenzymatic synthesis of carbasugars from iodobenzene
Boyd, Derek R.,Sharma, Narain D.,Llamas, Nuria M.,Malone, John F.,O'Dowd, Colin R.,Allen, Christopher C. R.
, p. 1953 - 1963 (2007/10/03)
The versatile enantiopure cis-dihydrodiol metabolite 1, formed by bacterial metabolism of iodobenzene, has been used for the synthesis of the pyranose carbasugars (pseudosugars) carba-β-D-altropyranose 2, carba-α-L- galactopyranose 3, carba-β-D-idopyranos
A norbornyl route to cyclohexitols: Structural diversity in fragmentation through functional group switching. Synthesis of α- and β- galactose, α-talose and α-fucopyranose carbasugars
Mehta, Goverdhan,Mohal, Narinder,Lakshminath, Sripada
, p. 3505 - 3508 (2007/10/03)
A novel fragmentation sequence has been executed within the norbornane system, involving C1-C7 bond scission, to extract a versatile, highly functionalized cyclohexanoid moiety. Its further evolution towards a range-of carbasugars is described. (C) 2000 Elsevier Science Ltd.
Strain-Directed Bridge Cleavage of (Phenylsulfonyl)-7-oxabicycloheptane Derivatives: Application to the Total Synthesis of Carba-α-DL-glucopyranose
Acena, Jose Luis,Arjona, Odon,Pradilla, Roberto Fernandez de la,Plumet, Joaquin,Viso, Alma
, p. 1945 - 1946 (2007/10/02)
New methodology to prepare highly oxygenated cyclohexenylsulfones by regioselective β-elimination of (phenylsulfonyl)-7-oxabicycloheptane derivatives has been developed, and its application to the total synthesis of carba-α-DL-glucopyranose is desc
SYNTHESIS OF FOUR NEW DIASTEREOISOMERS OF DL-5-HYDROXYMETHYL-1,2,3,4-CYCLOHEXANETETROL
Ogawa, Seiichiro,Tsukiboshi, Yoshiki,Iwasawa, Yoshikazu,Suami, Tetsuo
, p. 77 - 90 (2007/10/02)
Four new diastereoisomers of the pseudo-sugar DL-5-hydroxymethyl-1,2,3,4-cyclohexanetetrol, having (1,2,3,4/5)- (2), (1,5/2,3,4)- (3), (1,2,3/4,5)- (4), and (1,2,4,5/3)-configurations (5), have been synthesised by unambiguous sequences from readily availa
