Enantioselective Total Synthesis and Absolute Configuration Assignment of (+)‐Tronocarpine Enabled by an Asymmetric Michael/Aldol Reaction

Frontispiz: Enantioselective Total Synthesis and Absolute Configuration Assignment of (+)‐Tronocarpine Enabled by an Asymmetric Michael/Aldol Reaction

Angewandte Chemie ◽

10.1002/ange.202081061 ◽

2020 ◽

Vol 132 (10) ◽

Author(s):

Dong‐Xing Tan ◽

Jie Zhou ◽

Chao‐You Liu ◽

Fu‐She Han

Keyword(s):

Total Synthesis ◽

Absolute Configuration ◽

Aldol Reaction ◽

Enantioselective Total Synthesis and Absolute Configuration Assignment of (+)‐Tronocarpine Enabled by an Asymmetric Michael/Aldol Reaction

Angewandte Chemie International Edition ◽

10.1002/anie.201914868 ◽

2020 ◽

Vol 59 (10) ◽

pp. 3834-3839 ◽

Cited By ~ 8

Author(s):

Dong‐Xing Tan ◽

Jie Zhou ◽

Chao‐You Liu ◽

Fu‐She Han

Keyword(s):

Total Synthesis ◽

Absolute Configuration ◽

Aldol Reaction ◽

Frontispiece: Enantioselective Total Synthesis and Absolute Configuration Assignment of (+)‐Tronocarpine Enabled by an Asymmetric Michael/Aldol Reaction

Angewandte Chemie International Edition ◽

10.1002/anie.202081061 ◽

2020 ◽

Vol 59 (10) ◽

Author(s):

Dong‐Xing Tan ◽

Jie Zhou ◽

Chao‐You Liu ◽

Fu‐She Han

Keyword(s):

Total Synthesis ◽

Absolute Configuration ◽

Aldol Reaction ◽

Enantioselective Total Synthesis and Absolute Configuration Assignment of (+)-Toxicodenane A

Organic Letters ◽

10.1021/acs.orglett.1c03293 ◽

2021 ◽

Author(s):

Xu-Long Qin ◽

Guo-Jie Wu ◽

Fu-She Han

Keyword(s):

Total Synthesis ◽

Absolute Configuration ◽

Enantioselective total synthesis and structural assignment of callyspongiolide

Organic & Biomolecular Chemistry ◽

10.1039/c6ob02051h ◽

2016 ◽

Vol 14 (48) ◽

pp. 11357-11370 ◽

Cited By ~ 8

Author(s):

Arun K. Ghosh ◽

Luke A. Kassekert ◽

Joseph D. Bungard

Keyword(s):

Total Synthesis ◽

Absolute Configuration ◽

Structural Assignment ◽

Elucidation of absolute configuration, assignment of stereochemistry at the C-21 center and total synthesis of callyspongiolide are described.

First enantioselective total synthesis of both enantiomers of lancifolol. Correlation: absolute configuration/specific rotation

Tetrahedron Letters ◽

10.1016/s0040-4039(01)01202-3 ◽

2001 ◽

Vol 42 (35) ◽

pp. 6125-6128 ◽

Cited By ~ 5

Author(s):

Jean-Marie Galano ◽

Gérard Audran ◽

Honoré Monti

Keyword(s):

Total Synthesis ◽

Absolute Configuration ◽

Specific Rotation ◽

Enantioselective Total Synthesis

Enantioselective Total Synthesis and Determination of the Absolute Configuration of the 4,6,8,10,16,18-Hexamethyldocosane fromAntitrogus parvulus

European Journal of Organic Chemistry ◽

10.1002/ejoc.200700282 ◽

2007 ◽

Vol 2007 (21) ◽

pp. 3512-3519 ◽

Cited By ~ 37

Author(s):

Christian Herber ◽

Bernhard Breit

Keyword(s):

Total Synthesis ◽

Absolute Configuration ◽

The Absolute

A New Synthetic Approach to (+)-Hyacinthacine A1and the First Total Synthesis and Absolute Configuration Assignment of Naturally Occurring (+)-Hyacinthacine A6

European Journal of Organic Chemistry ◽

10.1002/ejoc.200700820 ◽

2007 ◽

Vol 2007 (36) ◽

pp. 6078-6083 ◽

Cited By ~ 17

Author(s):

Isidoro Izquierdo ◽

María T. Plaza ◽

Juan A. Tamayo ◽

Fernando Sánchez-Cantalejo

Keyword(s):

Total Synthesis ◽

Absolute Configuration ◽

Synthetic Approach ◽

Naturally Occurring ◽

Enantiospecific Total Synthesis and Absolute Configuration Assignment of Chabrolobenzoquinone H

The Journal of Organic Chemistry ◽

10.1021/acs.joc.1c02634 ◽

2021 ◽

Author(s):

Stergios R. Rizos ◽

Konstantinos A. Ouzounthanasis ◽

Alexandros E. Koumbis

Keyword(s):

Total Synthesis ◽

Absolute Configuration ◽

Enantioselective Total Synthesis of Chondrosterins I and J by Catalytic Asymmetric Intramolecular Aldol Reaction Using Chiral Diamine Catalyst

European Journal of Organic Chemistry ◽

10.1002/ejoc.202000579 ◽

2020 ◽

Vol 2020 (26) ◽

pp. 4050-4058

Author(s):

Yuichiro Kawamoto ◽

Daiki Ozone ◽

Toyoharu Kobayashi ◽

Hisanaka Ito

Keyword(s):

Total Synthesis ◽

Aldol Reaction ◽

Chiral Diamine ◽

Catalytic Asymmetric