Synthetic Studies Toward Pectenotoxin 2. Part I. Stereocontrolled Access to the C10−C22Fragment

2008 ◽  
Vol 10 (19) ◽  
pp. 4179-4182 ◽  
Author(s):  
Jatta E. Aho ◽  
Elina Salomäki ◽  
Kari Rissanen ◽  
Petri M. Pihko
Keyword(s):  
Synthetic Studies ◽  
Pectenotoxin 2

ChemInform Abstract: Synthetic Studies Toward Pectenotoxin 2. Part 1. Stereocontrolled Access to the C10-C22Fragment.

ChemInform ◽  
2009 ◽  
Vol 40 (6) ◽  
Author(s):  
Jatta E. Aho ◽  
Elina Salomaeki ◽  
Kari Rissanen ◽  
Petri M. Pihko
Keyword(s):  
Synthetic Studies ◽  
Pectenotoxin 2

Synthetic Studies towards Pectenotoxin-2: Synthesis of the Nonanomeric 10-epi-ABCDE Ring Segment by Kinetic Spiroketalization

2011 ◽  
Vol 2011 (9) ◽  
pp. 1682-1694 ◽  
Author(s):  
Jatta E. Aho ◽  
Antti Piisola ◽  
K. Syam Krishnan ◽  
Petri M. Pihko
Keyword(s):  
Ring Segment ◽  
Synthetic Studies ◽  
Pectenotoxin 2

Synthetic Studies Toward Pectenotoxin 2. Part II. Synthesis of the CDE and CDEF Ring Systems

2008 ◽  
Vol 10 (19) ◽  
pp. 4183-4185 ◽  
Author(s):  
Hannes Helmboldt ◽  
Jatta E. Aho ◽  
Petri M. Pihko
Keyword(s):  
Ring Systems ◽  
Synthetic Studies ◽  
Pectenotoxin 2

Pectenotoxin-2 Synthetic Studies. 3. Assessment of the Capacity for Stereocontrolled Cyclization To Form the Entire C1−C26 Subunit Based upon the Double Bond Geometry Across C15-C16

2007 ◽  
Vol 72 (5) ◽  
pp. 1747-1754 ◽  
Author(s):  
Patrick D. O'Connor ◽  
Christopher K. Knight ◽  
Dirk Friedrich ◽  
Xiaowen Peng ◽  
Leo A. Paquette
Keyword(s):  
Double Bond ◽  
Synthetic Studies ◽  
Pectenotoxin 2

Pectenotoxin-2 Synthetic Studies. 2. Construction and Conjoining of ABC and DE Eastern Hemisphere Subtargets

2005 ◽  
Vol 7 (9) ◽  
pp. 1813-1816 ◽  
Author(s):  
Dmitriy Bondar ◽  
Jian Liu ◽  
Thomas Müller ◽  
Leo A. Paquette
Keyword(s):  
Eastern Hemisphere ◽  
Synthetic Studies ◽  
Pectenotoxin 2

Synthetic studies toward inducamide C

2021 ◽  
Author(s):  
Ardalan A. Nabi ◽  
Lydia M. Scott ◽  
Daniel P. Furkert ◽  
Jonathan Sperry
Keyword(s):  
Natural Product ◽  
Structural Revision ◽  
Synthetic Studies

The rare benzoxazepine ring in the alkaloid inducamide C is unstable and prone to rearrangement, indicating that structural revision of the natural product may be necessary.

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