Photochemical Key Steps in Organic Synthesis. J. Mattay and A. Griesbeck, eds. VCH Weinheim, 1994. xi + 350 pp. DM 68.00/£ 27.50. ISBN 3-527-29214-4

2010 ◽  
Vol 115 (2) ◽  
pp. 154-155
Author(s):  
H.J.C. Jacobs
Keyword(s):  
Organic Synthesis ◽  
Key Steps

Synthetic approach to ryanodine; the use of O-spirodienone lactone in organic synthesis

1969 ◽  
Vol 47 (3) ◽  
pp. 515-519 ◽  
Author(s):  
Daniel Berney ◽  
Pierre Deslongchamps
Keyword(s):  
Organic Synthesis ◽  
Synthetic Approach ◽  
Key Steps

The key steps for this synthetic approach are the preparation of o-spirodienone lactone 15, its reaction with methylvinyl ketone which gave 16 and 17, and the conversion of 16 and 17 into compound 19 by base. Finally ozonolysis of 26 followed by internal condensation gave compound 28.

Photochemical Reactions as Key Steps in Organic Synthesis

2008 ◽  
Vol 108 (3) ◽  
pp. 1052-1103 ◽  
Author(s):  
Norbert Hoffmann
Keyword(s):  
Organic Synthesis ◽  
Photochemical Reactions ◽  
Key Steps

scholarly journals Synthesis of heterocyclic compounds using ring-closing enyne metathesis reaction

2020 ◽  
Vol 22 ◽  
pp. 20-29
Author(s):  
Titas Biswas ◽  
Keyword(s):  
Organic Synthesis ◽  
Heterocyclic Compounds ◽  
Enyne Metathesis ◽  
Metathesis Reaction ◽  
Molecular Complexity ◽  
The Creation ◽  
Key Steps

Ring-closing enyne metathesis reaction has emerged as an elegant tool in organic synthesis for the creation of molecular complexity and used to prepare diverse heterocycles. In this mini review, I discuss that various linearly and angularly architecture heterocyclic compounds may be prepared using RCEM as key steps.

ChemInform Abstract: Photochemical Key Steps in Organic Synthesis

ChemInform ◽  
2012 ◽  
Vol 43 (40) ◽  
pp. no-no
Author(s):  
Norbert Hoffmann
Keyword(s):  
Organic Synthesis ◽  
Key Steps
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