285 results on '"Reddy, Chada Raji"'
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2. Discovery of potent dual ligands for dopamine D4 and σ1 receptors
3. Iodo-Annulations of N -Benzyl-propiolamides Leading To Azaspiro[5.5]undecatrienones or Benzo[ c ]azepinones.
4. Photocatalytic Asymmetric Acyl Radical Truce–Smiles Rearrangement for the Synthesis of Enantioenriched α‐Aryl Amides.
5. Assembly of Functionalized 3,4‐Fused Tricyclic Benzosultams via Radical‐Promoted Cascade Reactions.
6. Bicyclic 5-6 Systems With One Bridgehead (Ring Junction) Nitrogen Atom: One Extra Heteroatom 1:0
7. Electrochemical selenylative ipso-annulation of N-benzylacrylamides to construct seleno-azaspiro [4.5]decadienones.
8. Carbonylative cyclization of biaryl enones with aldehydes and oxamic acids.
9. One-Pot Synthesis of N-Fused Benzimidazo-β-carbolines through Sequential Propargylation/aza-Cycloisomerization Approach
10. An entry to spiro-fused sultams via electrochemical brominative ipso-annulation of N-aryl alkynyl sulphonamides
11. Seleno/Thio-functionalized ipso-Annulation of N-Propiolyl-2-arylbenzimidazole to Construct Azaspiro[5,5]undecatrienones
12. Dearomative ipso-Cyclization to Spiropseudoindoxyls: An Extendable Approach To Access Indolo[3,2‑c]quinolinones and Isocryptolepine.
13. CAN-Promoted Thiolative ipso-Annulation of Unactivated N-Benzyl Acrylamides: Access to SCN/SCF3/SO2Ar Containing Azaspirocycles
14. Total synthesis of (+)-cladospolide D
15. Synthesis of the C8–C16 fragment of amphidinolide R
16. Structure Activity Relationship Studies around DB18, a Potent and Selective Inhibitor of CLK Kinases
17. ipso-Cyclization of unactivated biaryl ynones leading to thio-functionalized spirocyclic enones.
18. Aminative annulation of cyano-enynyl esters leading to functionalized cyclopentenones.
19. CAN-Promoted Thiolative ipso-Annulation of Unactivated N‑Benzyl Acrylamides: Access to SCN/SCF3/SO2Ar Containing Azaspirocycles.
20. Enantioselective access to (−)-indolizidines 167B, 209D, 239AB, 195B and (−)-monomorine from a common chiral synthon
21. A Sequential Cycloisomerization/Oxidative Aromatization of 2-Propargyl-cyclohexenones for Direct Access to Substituted Benzofurans
22. A Strategy for the Synthesis of Bicyclic Fused Cyclopentenones from MBH-Carbonates of Propiolaldehydes
23. Synthesis of (−)-dihydropinidine, (2 S,6 R)-isosolenopsin and (+)-monomorine via a chiral synthon from l-aspartic acid
24. Stereoselective synthesis of a tetrahydropyranyl diarylheptanoid, ent-diospongin A
25. A chiral pyrrolidine-pyrazole catalyst for the enantioselective Michael addition of carbonyls to nitroolefins
26. Synthesis and biological studies of new piperidino-1,2,3-triazole hybrids with 3-aryl isoxazole side chains
27. Hydroxyphthalimide allied triazole-pyrrolidine catalyst for asymmetric Michael additions in water
28. Proline–threonine dipeptide as an organocatalyst for the direct asymmetric aldol reaction
29. Novel Machaeriol Analogues as Modulators of Cannabinoid Receptors: Structure–Activity Relationships of (+)-Hexahydrocannabinoids and Their Isoform Selectivities
30. Iodo- and Chalcogenoannulation of Morita–Baylis–Hillman Alcohols of Propiolaldehydes: Entry to Functionalized 2-Pyrones
31. One-Pot Arylative Benzannulation of 2-Carbonyl-3-propargyl Indoles with Boronic Acids Leading to Arylated Carbazoles
32. Chemoenzymatic Process for the Preparation of (S)-7-((tert-Butyldiphenylsilyl)oxy)hept-1-yn-4-ol in a Continuous Packed-Bed Reactor, a Key Intermediate for Eribulin Synthesis
33. Ag-Catalyzed Oxidative ipso-Cyclization via Decarboxylative Acylation/Alkylation: Access to 3-Acyl/Alkyl-spiro[4.5]trienones
34. Oxa-[3+3] annulation of MBH-carbonates of propiolaldehydes with α-nitro/bromo ketones to access 2H-pyrans
35. Silver-catalyzed acylative annulation of N-propargylated indoles with α-keto acids: access to acylated pyrrolo[1,2-a]indoles
36. Synthesis and biological evaluation of longanlactone analogues as neurotrophic agents
37. A Facile Approach to 3,4‐Oxepino‐Fused Tricyclic Indoles from MBH‐Acetates of Acetylenic AldehydesviaSuccessive Allylic Substitution/Intramolecular [3+2] Annulation†
38. Facile Strategy to Access the Indolo[2,3-a]quinolizidine Framework: Synthetic Study on Tangutorine
39. One-Pot Synthesis of Triazolo-Heterolignans: Biological Evaluation and Molecular Docking Studies as Tubulin Inhibitors
40. Copper-Catalyzed Intramolecular Chalcogenoamination of Enynyl Azides: Synthesis of 5-Selenyl/Sulfenyl Nicotinates
41. Metal-free propargylation/aza-annulation approach to substituted β-carbolines and evaluation of their photophysical properties
42. One-Pot Arylative Benzannulation of 2‑Carbonyl-3-propargyl Indoles with Boronic Acids Leading to Arylated Carbazoles.
43. One-Pot Assembly of 3‑Hydroxycarbazoles via Uninterrupted Propargylation/Hydroxylative Benzannulation Reactions.
44. Cu(I)-Catalyzed Aminative Aza-Annulation of Enynyl Azide using N-Fluorobenzenesulfonimide: Synthesis of 5-Aminonicotinates
45. Oxidative Aza-Annulation of Enynyl Azides to 2-Keto/Formyl-1H-pyrroles
46. ipso-Cyclization: an emerging tool for multifunctional spirocyclohexadienones
47. Facile Strategy to Access the Indolo[2,3- a ]quinolizidine Framework: Synthetic Study on Tangutorine 1.
48. A Facile Approach to 3,4‐Oxepino‐Fused Tricyclic Indoles from MBH‐Acetates of Acetylenic Aldehydes via Successive Allylic Substitution/Intramolecular [3+2] Annulation†.
49. A Facile Approach to 3,4‐Oxepino‐Fused Tricyclic Indoles from MBH‐Acetates of Acetylenic Aldehydes via Successive Allylic Substitution/Intramolecular [3+2] Annulation†.
50. Facile Entry to 3,4-Dihydro-1H-pyrrolo[2,1-c][1,4]oxazines through theoxa-Pictet-Spengler Reaction
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