Comment on “Nomenclature, Chemical Abstracts Service Numbers, Isomer Enumeration, Ring Strain, and Stereochemistry: What Does Any of This Have to Do with an International Chemical Disarmament and Nonproliferation Treaty?”

2021 ◽  
Vol 98 (4) ◽  
pp. 1465-1467
Author(s):  
Christoph Rücker ◽  
Markus Meringer ◽  
Alfred Wassermann
2021 ◽  
Author(s):  
Deborah Hartmann ◽  
Sven Braner ◽  
Lutz Greb

Bis(perchlorocatecholato)silane and bidentate N,N- or N,P-heteroleptic donors form hexacoordinated complexes. Depending on the ring strain and hemilability in the adducts, Frustrated Lewis pair reactivity with aldehydes and catalytic ammonia borane...


1998 ◽  
Vol 63 (6) ◽  
pp. 2052-2052
Author(s):  
Nobuya Katagiri ◽  
Masahiro Takebayashi ◽  
Chikara Kaneko ◽  
Kouichi Kanehira ◽  
Masahiro Torihara

2000 ◽  
Vol 78 (6) ◽  
pp. 689-696 ◽  
Author(s):  
Jinsung Tae ◽  
Leo A Paquette

Highly functionalized and annulated 2,4-cyclooctadienones are formed in a stereoselective manner by sequential treatment of squarate esters with a lithiated enecarbamate (six-membered ring or larger) and a cycloalkenyl- or 1-alkenyllithium reagent. The mechanistic details of this multistep process are presented. Particular attention is drawn to the step that involves intramolecular nucleophilic attack by a proximal oxido anion at the carbamate carbonyl and results in redirection of the cascade. This step is thwarted when five-membered cyclic enecarbamates are employed because of the excessive buildup of ring strain in the associated transition state.Key words: squarate esters, enecarbamates, conrotatory ring opening, intramolecular acylation, alkenyllithium reagents.


1980 ◽  
Vol 20 (4) ◽  
pp. 193-201 ◽  
Author(s):  
Dale B. Baker ◽  
Jean W. Horiszny ◽  
Wladyslaw V. Metanomski

1990 ◽  
Vol 9 (3) ◽  
pp. 874-876 ◽  
Author(s):  
Jane K. Klassen ◽  
Gilbert K. Yang
Keyword(s):  

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