Recent Developments on the Total Synthesis of Nakadomarin A

2018 ◽  
Vol 3 (18) ◽  
pp. 5198-5206 ◽  
Author(s):  
Samaresh Jana ◽  
Habtamu Gelaw Mekonnen
Keyword(s):  
Total Synthesis ◽  
Nakadomarin A ◽  
Recent Developments

Total synthesis of (−)-nakadomarin A: alkyne ring-closing metathesis

2011 ◽  
Vol 52 (46) ◽  
pp. 6094-6097 ◽  
Author(s):  
Pavol Jakubec ◽  
Andrew F. Kyle ◽  
Jonás Calleja ◽  
Darren J. Dixon
Keyword(s):  
Total Synthesis ◽  
Ring Closing Metathesis ◽  
Nakadomarin A

scholarly journals Total Synthesis of (−)-Nakadomarin A

2010 ◽  
Vol 12 (21) ◽  
pp. 4912-4915 ◽  
Author(s):  
Mark G. Nilson ◽  
Raymond L. Funk
Keyword(s):  
Total Synthesis ◽  
Nakadomarin A

Total Synthesis Nakadomarin A

2003 ◽  
pp. 76
Author(s):  
Toshiaki Nagata ◽  
Masako Nakagawa ◽  
Atsushi Nishida
Keyword(s):  
Total Synthesis ◽  
Nakadomarin A

scholarly journals Halonium-Induced Polyene Cyclizations

Synthesis ◽  
2019 ◽  
Vol 51 (08) ◽  
pp. 1753-1769 ◽  
Author(s):  
Agathe D’Hollander ◽  
Laure Peilleron ◽  
Tatyana Grayfer ◽  
Kevin Cariou
Keyword(s):  
Natural Products ◽  
Total Synthesis ◽  
Asymmetric Reactions ◽  
Recent Developments ◽  
Halogenated Natural Products

This review covers the methods that chemists have developed to access halogenated polycyclic structures from polyenes, by emulating Nature’s enzymatic machineries. From pioneering studies to the most recent developments, the different strategies, whether based on the use of standard reagents or on the design of specific ones, will be presented. Finally, asymmetric reactions and applications for the total synthesis of natural products will be exposed.1 Introduction2 Pioneering Studies3 Use of Specific Reagents4 Use of N-Haloamides5 Asymmetric Reactions6 Total Synthesis of Halogenated Natural Products7 Conclusion and Perspectives

Total Synthesis of (+)-Nakadomarin A

2007 ◽  
Vol 129 (5) ◽  
pp. 1465-1469 ◽  
Author(s):  
Ian S. Young ◽  
Michael A. Kerr
Keyword(s):  
Total Synthesis ◽  
Nakadomarin A

scholarly journals The First Total Synthesis of Nakadomarin A [J. Am. Chem. Soc.2003,125, 7484−7485].

2003 ◽  
Vol 125 (44) ◽  
pp. 13618-13618 ◽  
Author(s):  
Toshiaki Nagata ◽  
Masako Nakagawa ◽  
Atsushi Nishida
Keyword(s):  
Total Synthesis ◽  
Nakadomarin A

A Review on Recent Developments in Syntheses of the post-Secodine Indole Alkaloids. Part II: Modified Alkaloid Types

2007 ◽  
Vol 72 (7) ◽  
pp. 821-898 ◽  
Author(s):  
Josef Hájíček
Keyword(s):  
Total Synthesis ◽  
Indole Alkaloids ◽  
Recent Developments ◽  
Lapidilectine B

The second part of the planned review on developments in the field of total and formal total synthesis of the post-secodine indole alkaloids concentrates on modified alkaloid types, i.e. those skeletons derived from primary types by formation of additional and/or rupture of existing bonds, while connectivities next to indol(e)ine moiety remain intact. It thus reviews the synthesis of alkaloids of quebrachamine/cleavamine type including VLB-bis-indoles, rhazinilam type, aspidofractinine/kopsane and kopsifoline type, as well as kopsijasminilam alkaloids, lapidilectine B and danuphylline. It covers the literature of from 1991-1992 up to approximately end 2006. A review with 174 references.

Synthesis of α-exo-Methylene-γ-butyrolactone: Recent Developments and Applications in Natural Product Synthesis

Synthesis ◽  
2021 ◽  
Author(s):  
Weilong Liu ◽  
Nicolas Winssinger
Keyword(s):  
Natural Products ◽  
Biological Activity ◽  
Total Synthesis ◽  
Natural Product ◽  
Natural Product Synthesis ◽  
Vast Array ◽  
The Past ◽  
New Approaches ◽  
Recent Developments

The α-exo-methylene-γ-butyrolactone moiety is present in a vast array of structurally diverse natural products and is often central to their biological activity. In this review, we summarize new approaches to α-exo-methylene-γ-butyrolactones developed over the past decade as well as their applications in total synthesis.

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