402475-58-5Relevant academic research and scientific papers
Total synthesis of carbocyclic nucleoside (+)-neplanocin A
Jung, Young Hoon,Kim, Seung In,Hong, Yeon Ju,Park, Sook Jin,Kang, Kyung Tae,Kim, So Yeon,Kim, In Su
, p. 1068 - 1073 (2015)
Asymmetric total synthesis of (+)-neplanocin A was concisely achieved from readily available d-galactose via the regioselective and diastereoselective amination of carbocyclic polybenzyl ether using chlorosulfonyl isocyanate and intramolecular olefin meta
Synthesis of L-cyclopentenyl nucleosides using ring-closing metathesis and palladium-mediated allylic alkylation methodologies
Agrofoglio, Luigi A.,Amblard, Franck,Nolan, Steven P.,Charamon, Steve,Gillaizeau, Isabelle,Zevaco, Thomas A.,Guenot, Pierre
, p. 8397 - 8404 (2004)
The enantiomeric synthesis of l-cyclopentenyl nucleosides is described. The key intermediate (+)-cyclopentenyl alcohol (8) was prepared from methyl-α-d-galactopyranoside 1 using a ring closing metathesis reaction. Transformation of the allylic alcohol 8 i
Divergent synthesis of aminocyclopentitol analogues via stereoselective amination of cyclic polybenzyl ether with chlorosulfonyl isocyanate
Jung, Young Hoon,Kim, Seung In,Hong, Yeon Ju,Park, Sook Jin,Kang, Kyung Tae,Kim, So Yeon,Park, Jung Sang,Kim, In Su
, p. 1089 - 1092 (2015/05/20)
Abstract The divergent synthesis of some novel aminocyclopentitol analogues was concisely achieved from readily available d-galactose via the highly diastereoselective amination of carbocyclic polybenzyl ether using chlorosulfonyl isocyanate, diastereosel
Baylis-Hillman reaction based flexible strategy for the synthesis of gabosine I, gabosine G, epi-gabosine i and carba l-pentose
Radha Krishna, Palakodety,Kadiyala, Raghu Ram
, p. 744 - 747 (2012/03/08)
A combination of diastereoselective Baylis-Hillman reaction and RCM reaction set is used as the flexible strategy for the ready access to cyclohexenoid and cyclopentenoid skeletons.
Enantioselective synthesis of carba-L-furanose precursors of carbanucleosides, using ring-closing metathesis
Gillaizeau, Isabelle,Charamon, Steve,Agrofoglio, Luigi A
, p. 8817 - 8819 (2007/10/03)
Carba-L-sugars were synthesized in seven steps from known tetra-O-benzyl-D-galactopyranose (3). The synthesis of cyclopentene ring has been accomplished via a ring-closing metathesis step. Schrock's catalyst was employed on the unique diene, key intermedi
