Enantioselective Total Synthesis of Eicosanoid and Its Congener, Using Organocatalytic Cyclopropanation, and Catalytic Asymmetric Transfer Hydrogenation Reactions as Key Steps

2008 ◽  
Vol 73 (13) ◽  
pp. 5198-5201 ◽  
Author(s):  
Gullapalli Kumaraswamy ◽  
Mogilisetti Padmaja
Keyword(s):  
Total Synthesis ◽  
Transfer Hydrogenation ◽  
Asymmetric Transfer Hydrogenation ◽  
Enantioselective Total Synthesis ◽  
Hydrogenation Reactions ◽  
Catalytic Asymmetric ◽  
Key Steps

scholarly journals Enantioselective total synthesis of decytospolide A and decytospolide B using an Achmatowicz reaction

2018 ◽  
Vol 16 (33) ◽  
pp. 5979-5986 ◽  
Author(s):  
Arun K. Ghosh ◽  
Hannah M. Simpson ◽  
Anne M. Veitschegger
Keyword(s):  
Total Synthesis ◽  
Transfer Hydrogenation ◽  
Enantioselective Total Synthesis ◽  
Key Steps ◽  
Enantioselective Syntheses

Enantioselective syntheses of decytospolides are described using an Achmatowicz rearrangement, transfer hydrogenation and Friedel–Crafts acylation as the key steps.

scholarly journals Enantioselective Total Synthesis of (−)‐Finerenone Using Asymmetric Transfer Hydrogenation

2020 ◽  
Vol 132 (51) ◽  
pp. 23307-23311
Author(s):  
Andreas Lerchen ◽  
Narasimhulu Gandhamsetty ◽  
Elliot H. E. Farrar ◽  
Nils Winter ◽  
Johannes Platzek ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Transfer Hydrogenation ◽  
Asymmetric Transfer Hydrogenation ◽  
Enantioselective Total Synthesis

scholarly journals Enantioselective Total Synthesis of (−)‐Finerenone Using Asymmetric Transfer Hydrogenation

2020 ◽  
Vol 59 (51) ◽  
pp. 23107-23111
Author(s):  
Andreas Lerchen ◽  
Narasimhulu Gandhamsetty ◽  
Elliot H. E. Farrar ◽  
Nils Winter ◽  
Johannes Platzek ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Transfer Hydrogenation ◽  
Asymmetric Transfer Hydrogenation ◽  
Enantioselective Total Synthesis

Total Synthesis of Resolvin T4

Synlett ◽  
2021 ◽  
Author(s):  
Narihito Ogawa ◽  
Kohei Arai ◽  
Yuichi Kobayashi
Keyword(s):  
Total Synthesis ◽  
Ring Opening ◽  
Transfer Hydrogenation ◽  
Asymmetric Transfer Hydrogenation ◽  
Ring Opening Reaction ◽  
Propargylic Alcohol ◽  
Chiral Centers ◽  
Wittig Reactions

AbstractA total synthesis of resolvin T4 was achieved by connecting three intermediates by Wittig reactions. The enal in the C1–C10 part was constructed through reduction of a propargylic alcohol with Red-Al followed by oxidation. The enal moiety in the C11–C16 part was synthesized by a ring-opening reaction of a silyl epoxide followed by a Peterson elimination. The chiral centers at C7 and C13 were constructed by ruthenium-catalyzed asymmetric transfer hydrogenation.

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