A Convergent Coupling Strategy for the Formation of Polycyclic Ethers: Stereoselective Synthesis of the BCDE Fragment of Brevetoxin A

Organic Letters ◽

10.1021/ol051543m ◽

2005 ◽

Vol 7 (18) ◽

pp. 4033-4036 ◽

Author(s):

Michael T. Crimmins ◽

Patrick J. McDougall ◽

Kyle A. Emmitte

Keyword(s):

Stereoselective Synthesis ◽

Brevetoxin A ◽

Coupling Strategy ◽

Polycyclic Ethers

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Stereoselective Synthesis of 2,6-syn-Dimethyl-tetrahydropyran Derivatives, Important Segments of Marine Polycyclic Ethers, by Unique Insertion of the Methyl Group

Organic Letters ◽

10.1021/ol9018419 ◽

2009 ◽

Vol 11 (21) ◽

pp. 4814-4817 ◽

Author(s):

Michihiro Maemoto ◽

Atsushi Kimishima ◽

Tadashi Nakata

Keyword(s):

Stereoselective Synthesis ◽

Methyl Group ◽

Polycyclic Ethers

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ChemInform Abstract: Enantioselective Total Synthesis of Brevetoxin A: Convergent Coupling Strategy and Completion.

10.1002/chin.200946215 ◽

2009 ◽

Vol 40 (46) ◽

Author(s):

Michael T. Crimmins ◽

J. Lucas Zuccarello ◽

Patrick J. McDougall ◽

J. Michael Ellis

Keyword(s):

Total Synthesis ◽

Enantioselective Total Synthesis ◽

Brevetoxin A ◽

Coupling Strategy

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ChemInform Abstract: Hydrostannylation-Cross-Coupling Strategy for the Stereoselective Synthesis of Alkylidenemalonates and Related α,β-Unsaturated Esters.

10.1002/chin.201525076 ◽

2015 ◽

Vol 46 (25) ◽

pp. no-no

Author(s):

Shinichi Fujiwara ◽

Romain Cadou ◽

Yousuke Yamaoka ◽

Kiyosei Takasu ◽

Ken-ichi Yamada

Keyword(s):

Stereoselective Synthesis ◽

Cross Coupling ◽

Unsaturated Esters ◽

Coupling Strategy

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ChemInform Abstract: Stereoselective Synthesis of the 6,7,6- and 6,7,7-Ring Systems of Polycyclic Ethers by 6-endo Cyclization and Ring Expansion.

10.1002/chin.199802249 ◽

2010 ◽

Vol 29 (2) ◽

pp. no-no

Author(s):

Y. MORI ◽

K. YAEGASHI ◽

H. FURUKAWA

Keyword(s):

Stereoselective Synthesis ◽

Ring Expansion ◽

Ring Systems ◽

Polycyclic Ethers

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Haem d1: stereoselective synthesis of the reduced form of its parent macrocycle using the original coupling strategy

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/a700652g ◽

1997 ◽

pp. 2099-2110 ◽

Author(s):

Christopher J. Aucken ◽

Finian J. Leeper ◽

Alan R. Battersby

Keyword(s):

Stereoselective Synthesis ◽

Reduced Form ◽

Coupling Strategy

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Stereoselective synthesis of the 6,7,6- and 6,7,7-ring systems of polycyclic ethers by 6-endo cyclization and ring expansion

Tetrahedron ◽

10.1016/s0040-4020(97)00816-8 ◽

1997 ◽

Vol 53 (38) ◽

pp. 12917-12932 ◽

Author(s):

Yuji Mori ◽

Keisuke Yaegashi ◽

Hiroshi Furukawa

Keyword(s):

Stereoselective Synthesis ◽

Ring Expansion ◽

Ring Systems ◽

Polycyclic Ethers

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Enantioselective Total Synthesis of Brevetoxin A: Convergent Coupling Strategy and Completion

Chemistry - A European Journal ◽

10.1002/chem.200900777 ◽

2009 ◽

Vol 15 (36) ◽

pp. 9235-9244 ◽

Author(s):

Michael T. Crimmins ◽

J. Lucas Zuccarello ◽

Patrick J. McDougall ◽

J. Michael Ellis

Keyword(s):

Total Synthesis ◽

Enantioselective Total Synthesis ◽

Brevetoxin A ◽

Coupling Strategy

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Nature Inspired Molecular Design: Stereoselective Synthesis of Bicyclic and Polycyclic Ethers for Potent HIV-1 Protease Inhibitors

Asian Journal of Organic Chemistry ◽

10.1002/ajoc.201800255 ◽

2018 ◽

Vol 7 (8) ◽

pp. 1448-1466 ◽

Author(s):

Arun K. Ghosh ◽

Margherita Brindisi

Keyword(s):

Protease Inhibitors ◽

Stereoselective Synthesis ◽

Molecular Design ◽

Polycyclic Ethers ◽

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ChemInform Abstract: Haem d1: Stereoselective Synthesis of the Reduced Form of Its Parent Macrocycle Using the Original Coupling Strategy.

10.1002/chin.199748144 ◽

2010 ◽

Vol 28 (48) ◽

pp. no-no

Author(s):

C. J. AUCKEN ◽

F. J. LEEPER ◽

A. R. BATTERSBY

Keyword(s):

Stereoselective Synthesis ◽

Reduced Form ◽

Coupling Strategy

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Stereoselective synthesis of alkyl-, aryl-, vinyl- and alkynyl-substituted Z-enamides and enol ethers

Chemical Science ◽

10.1039/c8sc05573d ◽

2019 ◽

Vol 10 (11) ◽

pp. 3223-3230 ◽

Author(s):

Paola Caramenti ◽

Nina Declas ◽

Romain Tessier ◽

Matthew D. Wodrich ◽

Jerome Waser

Keyword(s):

Natural Products ◽

Room Temperature ◽

Stereoselective Synthesis ◽

Cross Coupling ◽

Enol Ethers ◽

Coupling Strategy

Highly stereoselective synthesis of Z-enamides and enol ethers at room temperature via an umpolung/cross coupling strategy applicable to drugs and natural products.

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