about
Palladium-Catalyzed Intramolecular Trost-Oppolzer-Type Alder-Ene Reaction of Dienyl Acetates to Cyclopentadienes.Cyclopenta[b]annulation of Heteroarenes by Organocatalytic γ'[C(sp3 )-H] Functionalization of Ynones.Morita-Baylis-Hillman Reaction of β,β-Disubstituted Enones: An Enantioselective Organocatalytic Approach for the Synthesis of Cyclopenta[b]annulated Arenes and Heteroarenes.One-Pot Multicatalytic Approaches for the Synthesis of Cyclohepta[b]indoles, Indolotropones, and Tetrahydrocarbazoles.One-Pot Trimetallic Relay Catalysis: A Unified Approach for the Synthesis of β-Carbolines and Other [c]-Fused Pyridines.Organocatalytic β-Azidation of Enones Initiated by an Electron-Donor-Acceptor Complex.Organocatalytic Strategies for the Synthesis of Cyclopenta-Fused Arenes and HeteroarenesBeyond the Corey-Chaykovsky Reaction: Synthesis of Unusual Cyclopropanoids via Desymmetrization and ThereofMetal- and Hydride-Free Pentannulative Reductive Aldol ReactionSynthesis of Cyclopropanoids via Substrate-Based Cyclization PathwaysPhosphine- and water-promoted pentannulative aldol reactionSubstituent-Guided Palladium-Ene Reaction for the Synthesis of Carbazoles and Cyclopenta[ b]indolesRing-Opening/Recyclization Cascades of Monoactivated Cyclopropanes
P50
Q48153533-40A578EF-7C6B-4D66-9903-0F856FC8FB4FQ48265235-BC3E92AC-64C9-4C80-ACA6-6371B2F2869FQ48275940-F7EF8709-0CC2-4EEB-96AC-FF27224FBAB2Q48278680-05A3BA2E-3552-4301-B49A-6B7CA1CA6371Q50871520-81C3E706-6E8B-456E-8FAE-A852BBCC7062Q52489685-0618C5F4-F032-4E97-8232-B5F226473BE6Q88410122-246D03E4-0E48-4A6E-9760-441FBB33D334Q90075542-7EE0A10D-095F-43EB-9DB9-C18B9B51F7AEQ90447828-7BD5242A-8F72-4711-9ED0-912F3B8CD925Q90447859-000BC7E2-DDE1-4C74-AC61-3AC7665882A3Q91246830-BDE6C026-D53C-4A13-B6F0-A1079D7EE3DEQ93092565-7D4591AE-0E2F-41DE-922D-F3C3233AAE1CQ93206663-E6459225-093E-4CA6-969F-06AB6867A5D2
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
S S V Ramasastry
@en
S S V Ramasastry
@nl
type
label
S S V Ramasastry
@en
S S V Ramasastry
@nl
prefLabel
S S V Ramasastry
@en
S S V Ramasastry
@nl
P31
P496
0000-0001-5814-9092