Morin, Marie 1649-1730

Histoire simple et véritable : les annales de l'Hôtel-Dieu de Montréal, 1659-1725 by Marie Morin( Book )

22 editions published between 1921 and 1994 in French and English and held by 89 WorldCat member libraries worldwide

Cette édition critique offre pour la première fois, après une adaptation partielle en 1921, le texte intégral du premier écrivain né en Nouvelle-France. "A l'histoire de la communauté de Montréal et de l'Hôtel-Dieu, s'ajoute l'histoire de Montréal, sa fondation et son établissement, son développement entrecoupé des guerres iroquoises et des tentatives d'invasion anglaises" (introd., p. xiii). Les notes critiques figurent à la fin de l'ouvrage

Mémoires de la Société historique de Montréal by Société historique de Montréal( Book )

9 editions published between 1921 and 2018 in French and held by 35 WorldCat member libraries worldwide

Mémoires de la Société historique de Montréal by Marie Morin( Book )

2 editions published in 1921 in French and held by 10 WorldCat member libraries worldwide

The Atalantium trilogy by Marie Morin( Book )

2 editions published in 2004 in English and held by 6 WorldCat member libraries worldwide

Bride of Atlantis by Marie Morin( )

1 edition published in 2003 in English and held by 6 WorldCat member libraries worldwide

Annales de l'Hôtel-Dieu de Montréal redigées by Marie Morin( Book )

1 edition published in 1921 in French and held by 3 WorldCat member libraries worldwide

Applications of new phosphorus-based 1,3-dipolar cycloaddition reagents in nitrogen heterocycle synthesis by Marie Morin( )

1 edition published in 2013 in English and held by 3 WorldCat member libraries worldwide

"This thesis describes the study of phospha-Münchnones, a new class of 1,3-dipole. These 1,3-dipoles have been previously demonstrated to be accessible in a one-pot reaction of imines, acid chlorides and organophosphorus reagents, and participate in 1,3-dipolar cycloaddition reactions. The objective of the research described in this thesis is to both understand the reactivity of these dipoles, and exploit their cycloaddition with alkynes and alkenes to synthesize pyrroles and 2-pyrrolines with high regio-, diastereo- and enantioselectivity. Chapter 2 focuses on understanding the factors that control regioselectivity in 1,3-dipolar cycloaddition reactions of phospha-Münchnones with alkynes, as well as the related mesoionic heterocycles Münchnones and Münchnone-imines. While each of the dipoles are established to participate in 1,3-dipolar cycloaddition reactions, until now, no general rules regarding the factors that control regioselectivity have been described. Cycloaddition reactions of the above mentioned dipoles are examined with a range of unsymmetrical electron poor and electron rich alkynes, and by comparing the behavior of these related dipoles, trends are observed in regioselectivity that relates to the alkyne ionization potential. In conjunction with Prof. Houk and Dr. Krenske at UCLA, DFT calculations were performed that provides a rational for the different behaviors of each of these dipoles. Importantly, these 1,3-dipoles display divergent regioselectivity, which can be exploited to synthesize a variety of pyrroles with high selectivity through the use of the appropriate reactant. Similarly, the rational on regioselectivity also allows the prediction of regioselectivity for a wide scope of alkynes. In Chapter 3 we explore the effect of the organophosphorus unit in phospha-Münchnones on their structure, reactivity and regioselectivity. X-ray crystallographic studies demonstrate the significant role of the PR3 unit on the ground state structure of these dipoles and their reactivity. In addition, the results of the theoretical investigation of Chapter 2 are exploited to show how changes in the phosphorus substituents can be used to fine tune regioselectivity of alkyne cycloadditions without modifying the substituents on the final product. In Chapter 4, phospha-Münchnone cycloaddition with alkenes is explored. Different phosphites and phosphonites are tested for their ability to mediate intramolecular cycloaddition with alkenes, and optimum results are obtained with (2-catechyl)PPh. Polycyclic 2-pyrrolines are generated in rapid cycloaddition reactions, in a modular fashion from easily accessible starting materials: olefin-tethered imines, acid chlorides and phosphonites. In addition, the reaction proceeds with high diastereo- and regioselectivity. The utility of this reaction has been extended to other products, including in situ reduction of the 2-pyrroline to pyrolidines, or oxidation to form pyrroles. In Chapter 5, a new way to control the enantioselectivity in 1,3-dipolar cycloaddition reactions is described. By the use of (R)-BINOL-based phosphites, a phospha-Münchnone can be prepared that is easily accessible, modular, yet requires no additional steps to install or remove the chiral fragment. As such, this provides a straightforward approach to control chirality in 1,3-dipolar cycloaddition reactions. This has been used to generate polycyclic pyrrolines and pyrrolidines with three or four stereogenic centers in one pot, and up to 99% ee."--

Orgasmizer9000 : and other stories by Angelique Anjou( Book )

1 edition published in 2005 in English and held by 3 WorldCat member libraries worldwide

Vetas de plata en Chihuahua( Book )

1 edition published in 2005 in Spanish and held by 2 WorldCat member libraries worldwide

Annales de l'hotel-dieu de montreal, 1921 (classic reprint) by MARIE MORIN( Book )

1 edition published in 2017 in French and held by 2 WorldCat member libraries worldwide