Pierre Soucy

Université de Sherbrooke

Author Statistics

Papers

Citation

H-Index

i-10 index

Research Trends

Author Order

Document Type

Co-Authors

Pierre Deslongchamps

Université Laval

Luc Ruest

Université de Sherbrooke

Richard Lapalme

Université de Sherbrooke

H.‐J. BORSCHBERG

ETH Zurich

Daniel Berney

Colorado State University

Alain Doutheau

École d'Ingénieurs en Chimie et Sciences du Numérique

Hajime Katayama

Geological Survey of Japan

Louiselle Saint-Laurent

Université de Sherbrooke

Fabrizio Marazza

Cerbios (Switzerland)

Robert Martino

Molécules d'Intérêt Biologique

Cooperative Institutions

Université de Sherbrooke

Université Laval

Centre National de la Recherche Scientifique

McGill University

Université de Montréal

Hôpital Fleurimont

University of Toronto

OmegaChem (Canada)

ETH Zurich

Board of the Swiss Federal Institutes of Technology

Author Statistics

Papers

Citation

H-Index

i-10 index

Research Field

CCDC 600997: Experimental Crystal Structure Determination

The Cambridge Structural Database (2006)

Sreekanth A. Ramachandran Rajendra K. Kharul Sylvain R. A. Marque Pierre Soucy Frédéric Jacques

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

10.5517/ccn5d06

Cite

Citations (0)

ChemInform Abstract: A CONVENIENT SYNTHESIS OF TRIQUINACENE‐2‐CARBOXYLIC ACID AND A NEW APPROACH TOWARDS THE SYNTHESIS OF DODECAHEDRANE

Chemischer Informationsdienst (1982)

Pierre Deslongchamps Pierre Soucy

Abstract Ausgehend von der Säure (I) wird über die Stufen (IIa)+(IIb) [Überführung bekannt], (IIIa)+(IIIb), (IV), (V21) und (Vb) ′ die rac. Trichinan‐carbonsätire (Vc) synthetisiert.

10.1002/chin.198217140

Cite

Citations (0)

The total synthesis of (+)-ryanodol. Part IV. Preparation of (+)-ryanodol from (+)-anhydroryanodol

Canadian Journal of Chemistry (1990)

Pierre Deslongchamps André Bélanger Daniel Berney Hans‐Jürg Borschberg Robert Brousseau

This paper reports the transformation of (+)-anhydroryanodol (6) to (+)-ryanodol (7) by reductive cyclization of lactone epoxide derivatives 9 and 20 (Scheme 4). Keywords: anhydroryanodol, ryanodol, diterpene, synthesis, reductive cyclization.

10.1139/v90-024

Cite

Citations (32)

ChemInform Abstract: OX. VON CYCLISCHEN KETONEN MIT CERAMMONIUMNITRAT

Chemischer Informationsdienst (1972)

Pierre Soucy Tse‐Lok Ho Pierre Deslongchamps

Abstract Die Oxidation cyclischer Ketone wie z.B. (I) und (VI) mit Ce‐ammoniumnitrat in wäßrigem Acetonitril bei 60°C führt zu Nitratocarbonsäurederivaten wie den Estern (II)‐(V) bzw. der cis‐ und trans‐Säure (VII).

10.1002/chin.197244125

Cite

Citations (0)

ChemInform Abstract: Selective Synthesis of trans‐anti‐cis (TAC) or cis‐anti‐trans (CAT) Tricycles from the Transannular Diels‐Alder of TTT Macrocyclic Trienes.

ChemInform (1994)

Pierre Soucy Yves L. Dory Pierre Deslongchamps

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

Cis–trans isomerism

10.1002/chin.199438054

Cite

Citations (0)

ChemInform Abstract: First Transannular Diels‐Alder Reactions Involving Tetrasubstituted Non‐Activated Dienophiles.

ChemInform (1995)

Jacques Y. Roberge Pascall Giguère Pierre Soucy Yves L. Dory Pierre Deslongchamps

Diels–Alder reaction

10.1002/chin.199512258

Cite

Citations (0)

Pyranophane Transannular Diels—Alder Approach to (+)‐Chatancin (I): A Biomimetic Asymmetric Total Synthesis.

ChemInform (2004)

Pierre Soucy Alexandre L’Heureux András Toró Pierre Deslongchamps

10.1002/chin.200421174

Cite

Citations (0)

Transannular Diels–Alder reactions on 14-membered macrocyclic trienes. Part I: stereoselective syntheses of the macrocyclic trienes precursors

Canadian Journal of Chemistry (1993)

Alexis Ndibwami Serge Lamothe Daniel Guay Raymond Plante Pierre Soucy

Transannular Diels–Alder reactions on 14-membered macrocycles containing properly located diene and methyl-substituted dienophile units lead to A.B.C.[6.6.6] tricycles related to steroids. To study the influence of the olefin and diene geometry on the stereochemical outcome of the Diels–Alder reaction it was necessary to prepare macrocyclic trienes of well-defined stereochemistry. Eight different types of macrocyclic trienes might be obtained by the coupling of appropriate dienophiles and dienes, namely, TTC, TTT, TCC, TCT, CTC, CTT, CCC, and CCT. In this paper (first in a series of two), the synthesis of appropriately functionalized dienophile and diene synthons, as well as their coupling reaction affording macrocyclic triene precursors, is described.

Synthon

Diene

Diels–Alder reaction

10.1139/v93-094

Cite

Citations (15)

A Convenient Synthesis of Triquinacene

Synthetic Communications (1973)

C. Mercier Pierre Soucy William Rosen Pierre Deslongchamps

Abstract We have recently reported the synthesis of a derivative of triquinacene (2,3-dihydrotriquinacen-2-one (14)4) from Thiele's acid (1). Although this new synthetic route is simple in concept, it suffers from a large number of chemical steps. We wish to communicate an important overall simplification of this synthetic scheme which makes readily available triquinacene (22) and several of its derivatives.

Derivative (finance)

10.1080/00397917308062026

Cite

Citations (28)

Formal total synthesis of erythromycin A. Part III. Synthesis of Woodward's carbamate key intermediate from a 1,7-dioxaspiro[5.5]undecane derivative of erythronolide A

Canadian Journal of Chemistry (1985)

Bruno Bernet Paul M. Bishop Maurice Caron Takeshi Kawamata Bernard L. Roy

The spirocompound 1 which was obtained by total synthesis (Part I) and by degradation from erythromycin (Part II) was converted into carbamate product 15, a key intermediate in the Woodward's total synthesis of erythromycin A.

Undecane

Carbamate

Derivative (finance)

10.1139/v85-470

Cite

Citations (18)