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Index « Auteurs » - entrée « Ata Martin Lawson »
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List of bibliographic references indexed by Ata Martin Lawson

Number of relevant bibliographic references: 7.
Ident.Authors (with country if any)Title
000046 (2016) Thomas Lepitre [France] ; Clement Denhez [France] ; Morgane Sanselme [France] ; Mohamed Othman [France] ; Ata Martin Lawson [France] ; Adam Daïch [France]Original Mitsunobu-Triggered Sequence Involved in a One-Pot Domino Process toward Tetracyclic Systems Bearing a Bis-N,O-acetal Junction.
000160 (2015) Ronan Le Goff [France] ; Arnaud Martel ; Morgane Sanselme ; Ata Martin Lawson ; Adam Daïch ; Sébastien ComesseSimple access to highly functional bicyclic γ- and δ-lactams: origins of chirality transfer to contiguous tertiary/quaternary stereocenters assessed by DFT.
000171 (2015) Aymen Ben Nejma [Tunisie] ; Asma Nguir [Tunisie] ; Hichem Ben Jannet [Tunisie] ; M'Hamed Ali Hamza [Tunisie] ; Adam Daïch [France] ; Mohamed Othman [France] ; Ata Martin Lawson [France]New septanoside and 20-hydroxyecdysone septanoside derivative from Atriplex portulacoides roots with preliminary biological activities.
000456 (2013) Ronan Le Goff [France] ; Ata Martin Lawson ; Adam Daïch ; Sébastien ComesseSynthesis of highly functionalized pyrrolidines as tunable templates for the direct access to (±)-coerulescine and the tricyclic core of martinellines.
000515 (2013) Meral Goermen ; Ronan Le Goff ; Ata Martin Lawson ; Adam Daich ; Sebastien ComesseChemInform Abstract: Tandem Aza‐Michael/Spiro‐Ring Closure Sequence: Access to a Versatile Scaffold and Total Synthesis of (.+‐.)‐Coerulescine.
000516 (2013) Ronan Le Goff ; Ata Martin Lawson ; Adam Daich ; Sebastien ComesseChemInform Abstract: Synthesis of Highly Functionalized Pyrrolidines as Tunable Templates for the Direct Access to (.+‐.)‐Coerulescine and the Tricyclic Core of Martinellines.
000518 (2013) Catalin Pintiala ; Ata Martin Lawson ; Sebastien Comesse ; Adam DaichChemInform Abstract: A Versatile Domino Process for the Synthesis of Substituted 3‐Aminomethylene‐chromanones and 2‐Pyridones Catalyzed by CsF.

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