Articles citing this paper
Multiple Carbon Bond Formation Via the Radical Cyclization of Cycloalkenol Acetals. Application to trans Hydrindan Steroid Precursors
G Stork and PJ Franklin
45(1) pp.275 - 284
10 articles found in Crossref database.
Approach towards an EPC synthesis of nodusmicin. Part 5: 1 Stereoselective introduction of a side chain at the cis -decalin part of nodusmicin
Gössinger Edda,
Schwartz Alexander, Sereinig Natascha
Tetrahedron. 2001 57(15). p.3045
Synthesis of (±)- and (−)-botryodiplodin using stereoselective radical cyclizations of acyclic esters and acetals
Nouguier Robert,
Gastaldi Stéphane,
Stien Didier,
Bertrand Michèle,
Villar Félix,
Andrey Olivier, Renaud Philippe
Tetrahedron: Asymmetry. 2003 14(19). p.3005
Enantioselective synthesis of steroids
Chapelon Anne-Sophie,
Moraléda Delphine,
Rodriguez Raphaël,
Ollivier Cyril, Santelli Maurice
Tetrahedron. 2007 63(47). p.11511
Highly Stereoselective Radical Cyclization of Haloacetals Controlled by the Acetal Center
Villar Félix,
Kolly‐Kovac Tanja,
Equey Olivier, Renaud Philippe
Chemistry – A European Journal. 2003 9(7). p.1566
Synthesis of DOHNAA, a Mycobacterium tuberculosis Cholesterol CD Ring Catabolite and FadD3 Substrate
Stubbing Louise A.,
Lott J. Shaun,
Dawes Stephanie S.,
Furkert Daniel P., Brimble Margaret A.
European Journal of Organic Chemistry. 2015 2015(27). p.6075
ChemInform Abstract: Multiple Carbon Bond Formation via the Radical Cyclization of Cycloalkenol Acetals. Application to trans Hydrindan Steroid Precursors.
STORK G., FRANKLIN P. J.
ChemInform. 1992 23(16).
Stereoselective SN2′ alkylation reaction sequence of the γ,δ-epoxy α,β-unsaturated ester system via γ,δ-chlorohydrin intermediates by the use of a R3Al–CuCN reagent
Yoshimura Fumihiko,
Matsui Atsushi,
Hirai Atsushi,
Tanino Keiji, Miyashita Masaaki
Tetrahedron Letters. 2009 50(36). p.5126
A simple strategy for the synthesis of optically pure trans-hydrindane systems
Pandey Ganesh, Raikar Sanjay B.
Tetrahedron Letters. 2006 47(12). p.2029
Intramolecular homolytic substitution at the sulfur atom: an alternative way to generate phosphorus- and sulfur-centered radicals
Carta Paola,
Puljic Nicolas,
Robert Carine,
Dhimane Anne-Lise,
Ollivier Cyril,
Fensterbank Louis,
Lacôte Emmanuel, Malacria Max
Tetrahedron. 2008 64(52). p.11865
Der Stand der Totalsynthese zu Beginn des 21. Jahrhunderts
Nicolaou K. C.,
Vourloumis Dionisios,
Winssinger Nicolas, Baran Phil S.
Angewandte Chemie. 2000 112(1). p.46
