612819-77-9Relevant academic research and scientific papers
Exploring functional and molecular diversity with polymer-bound p-alkoxybenzyl ethers - Scope and applicaitons of preparatively useful organic reactions
Hanessian, Stephen,Xie, Fang
, p. 737 - 740 (1998)
Alcohols immobilized as p-alkoxybenzyl ethers on Wang resins have been subjected to a variety of chemical transformations based on existing functionality (enolate chemistry, carbonyl group reactivity, Mitsunobu inversion, ozonolysis, Heck reactions, etc.), in an effort to test the suitability of this novel resin-bound ether linkage. The modified substrate was released from the resin by mild acid treatment.
Studies for the transformation of carbocycles into carbohydrates: Approach toward the synthesis of higher sugar derivatives
Baptistella, Lucia Helena Brito,Cerchiaro, Giselle
, p. 665 - 671 (2007/10/03)
A highly stereocontrolled synthesis of a β-D-ribo-hept-6- ulopyranosuronamide derivative, a useful intermediate for the synthesis of other higher sugars, has been developed using naturally occurring (-)-quinic acid as a chiral starting material. The trans
Total syntheses of aminomethyl-C-dideoxyglycopyranosides and their quinamides
Gremyachinskiy, Dmitriy E.,Samoshin, Vyacheslav V.,Gross, Paul H.
, p. 6587 - 6590 (2007/10/03)
Lewis acid promoted cyclization of homoallylic alcohol 1 with acetal 2 gave 4-chloro-2-phthalimidomethyl-6-methyltetrahydropyrans. Their dehydrochlorination produced two regioisomeric dihydropyrans. Subsequent cis- and trans-dihydroxylation gave four race
