Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Santosh Ramdas Borkar"'
Publikováno v:
Tetrahedron: Asymmetry. 28:186-195
A series of threo - and erythro -configured open-chain trihydroxy ketones was synthesized starting from l - and d -ascorbic acid respectively as the starting material, through the use of Grignard reactions for the requisite C C bond formations. The l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bf7a0412687a4ae3a042d1a60f6e070
https://doi.org/10.1016/j.tetasy.2016.11.008
https://doi.org/10.1016/j.tetasy.2016.11.008
Facile Formation of 5-Acylated-2-hydroxymethyl-furans from Open Chain D-Glucosyl-Alkyl/ Aryl Ketones
Publikováno v:
ChemistrySelect. 1:6004-6007
Open chain D-glucosyl alkyl/aryl ketones synthesized from readily available D-gluco-configured building block, under acidic conditions, cyclize to hitherto inaccessible 5-acylated-2-hydroxymethyl-furans in moderate to good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e10008f495a76593ffaed9698cce7d2
https://doi.org/10.1002/slct.201601599
https://doi.org/10.1002/slct.201601599
Publikováno v:
Carbohydrate research.
Total synthesis of naturally occurring Oxylipin has been achieved from open chain gluco-configured building block which is readily assembled from inexpensive and commercially available D-(+)-gluconolactone. Grignard reaction and Wittig olefination re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c29bed1eb8db16a40f11ab7af3c608d9
https://pubmed.ncbi.nlm.nih.gov/28319683
https://pubmed.ncbi.nlm.nih.gov/28319683
Publikováno v:
IndraStra Global.
This work focuses on the molecular level understanding of interaction between FTY720 (Fingolimod hydrochloride) and dimyristoylphosphatidylcholine (DMPC) multilamellar vesicles (MLVs) as a drug molecule carrier by investigating the structural changes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c44c00b65ab228b0e621807c2e002eb8
http://hdl.handle.net/11717/15534
http://hdl.handle.net/11717/15534
Publikováno v:
IndraStra Global.
D-gluco-Configured building block derived from d-(+)-gluconolactone has served as a common chiral template for the synthesis of enantiopure d- and l-xylo-configured 1,2,3,4-alkane tetrols. This has enabled synthesis of medicinally important guggultet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ab27a87fe77ebb813187043f62c0be4