144 results on '"Ghosh, Arun K"'
Search Results
2. A convenient synthesis of (3S,3aR,5R,7aS,8S)-Hexahydro-4H-3,5-methanofuro[2,3-b]pyran-8-ol, a high-affinity nonpeptidyl ligand for highly potent HIV-1 protease inhibitors
3. Highly diastereoselective asymmetric syn-aldol reactions of (R)-(N-tosyl)phenylalaninol propionate-derived titanium enolate and bidentate aromatic and aliphatic aldehydes
4. Synthesis of amide derivatives for electron deficient amines and functionalized carboxylic acids using EDC and DMAP and a catalytic amount of HOBt as the coupling reagents
5. Highly stereoselective asymmetric aldol routes to tert-butyl-2-(3,5-difluorophenyl)-1-oxiran-2-yl)ethyl)carbamates: Building blocks for novel protease inhibitors
6. An enantioselective enzymatic desymmetrization route to hexahydro-4H-furopyranol, a high-affinity ligand for HIV-1 protease inhibitors
7. An enantioselective synthesis of the C3–C21 segment of the macrolide immunosuppressive agent FR252921
8. TiCl 4 promoted three component coupling reaction: an efficient method for the substituted tetrahydropyrilidene acetates
9. TiCl 4 promoted three component coupling reaction: A new method for the synthesis of functionalized tetrahydrofurans and tetrahydropyrans
10. Enantioselective synthesis of dioxatriquinane structural motifs for HIV-1 protease inhibitors using a cascade radical cyclization
11. An enantioselective synthesis of a MEM-protected aetheramide A derivative
12. FeCl3-catalyzed tandem Prins and Friedel–Crafts cyclization: a highly diastereoselective route to polycyclic ring structures
13. Bifunctional cinchona alkaloid-squaramide-catalyzed highly enantioselective aza-Michael addition of indolines to α,β-unsaturated ketones
14. Enantioselective synthesis of spiro[cyclohexane-1,3′-indolin]-2′-ones containing multiple stereocenters via organocatalytic Michael/aldol cascade reactions
15. A tandem olefin migration and Prins cyclization using Cu(OTf)2–bisphosphine complexes: an improved synthesis of functionalized tetrahydropyrans
16. Synthesis of functionalized 4-methylenetetrahydropyrans by oxidative activation of cinnamyl or benzyl ethers
17. Stereoselective synthesis of the C 1–C 12 segment of iriomoteolide- 1a: a very potent macrolide antitumor agent
18. Enantioselective synthesis of cyclopentyltetrahydrofuran (Cp-THF), an important high-affinity P2-ligand for HIV-1 protease inhibitors
19. Stereoselective synthesis of the C1–C12 segment of iriomoteolide-1a: a very potent macrolide antitumor agent
20. Corrigendum to “Enantioselective synthesis of cyclopentyltetrahydrofuran (Cp-THF), an important high-affinity P2-ligand for HIV-1 protease inhibitors”
21. Synthetic studies of microtubule stabilizing agent peloruside A: an asymmetric synthesis of C10C24 segment
22. An enantioselective synthesis of the C1C9 segment of antitumor macrolide peloruside A
23. Chelation-controlled ester-derived titanium enolate aldol reaction: diastereoselective syn-aldols with mono- and bidentate aldehydes
24. Asymmetric hetero Diels–Alder route to quaternary carbon centers: synthesis of (−)-malyngolide
25. A macrolactonization-based strategy to obtain microtuble-stabilizing agent (−)-laulimalide
26. Ester derived titanium enolate aldol reaction: chelation controlled diastereoselective synthesis of syn -aldols
27. Stereoselective construction of quaternary carbon centers by three component coupling reactions
28. Synthetic studies of antitumor macrolide laulimalide: a stereoselective synthesis of the C17–C28 segment
29. An enantioselective synthesis of the C2–C16 segment of antitumor macrolide laulimalide
30. A stereoselective synthesis of (+)-boronolide
31. TiCl4 promoted three component coupling reaction: an efficient method for the substituted tetrahydropyrilidene acetates
32. TiCl4 promoted three component coupling reaction: A new method for the synthesis of functionalized tetrahydrofurans and tetrahydropyrans
33. Stereoselective synthesis of dihydroisocoumarin moiety of microbial agent AI-77-B: a Diels-Alder based strategy
34. Ring-closing metathesis strategy to unsaturated γ- and δ-lactones: Synthesis of hydroxyethylene isostere for protease inhibitors
35. Convenient synthesis of novel macrocyclic urethanes: alkoxycarbonylation of amines and ring-closing metathesis strategy
36. Chemoselective catalytic hydrogenation of alkenes by Lindlar catalyst
37. Ester derived titanium enolate aldol reaction: Highly diastereoselective synthesis of syn- and anti-aldols
38. SYNTHETIC STUDIES OF ANTITUMOR MACROLIDE LAULIMALIDE: ENANTIOSELECTIVE SYNTHESIS OF THE C3-C14 SEGMENT BY A CATALYTIC HETERO DIELS-ALDER STRATEGY
39. Conformationally constrained bis(oxazoline) derived chiral catalyst: A highly effective enantioselective Diels-Alder reaction
40. Synthesis and optical resolution of high affinity P2-ligands for HIV-1 protease inhibitors
41. Intramolecular and intermolecular hydroxyl reactivity differences in ginkgolides A, B and C and their chemical applications
42. N,N`-dissuccinimidyl carbonate: a useful reagent for alkoxycarbonylation of amines
43. Stereoselective reduction of α-hydroxy oxime ethers: a convenient route to cis1,2-amino alcohols
44. Di(2-pyridyl) carbonate promoted alkoxycarbonylation of amines: A convenient synthesis of functionalized carbamates
45. Synthetic studies of microtubule stabilizing agent peloruside A: an asymmetric synthesis of C 10C 24 segment
46. An enantioselective synthesis of the C 1C 9 segment of antitumor macrolide peloruside A
47. Synthetic studies of antitumor macrolide laulimalide: a stereoselective synthesis of the C 17–C 28 segment
48. An enantioselective synthesis of the C 2–C 16 segment of antitumor macrolide laulimalide
49. TiCl 4promoted three component coupling reaction: an efficient method for the substituted tetrahydropyrilidene acetates
50. TiCl 4promoted three component coupling reaction: A new method for the synthesis of functionalized tetrahydrofurans and tetrahydropyrans
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.