The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Jul. 18, 2017

Filed:

May. 02, 2016
Applicant:

The Florida State University Research Foundation, Inc., Tallahassee, FL (US);

Inventors:

Igor V. Alabugin, Tallahassee, FL (US);

Sayantan Mondal, Tallahassee, FL (US);

Rana K. Mohamed, Tallahassee, FL (US);

Attorney:
Primary Examiner:
Int. Cl.
CPC ...
C07C 17/093 (2006.01); C07C 29/42 (2006.01); C07F 7/22 (2006.01); C07C 1/32 (2006.01); C07C 45/00 (2006.01); C07D 333/08 (2006.01); C07D 213/16 (2006.01); C07D 239/26 (2006.01); C07C 253/30 (2006.01); C07C 41/01 (2006.01); C07C 41/16 (2006.01); C07C 41/30 (2006.01); C07C 67/333 (2006.01);
U.S. Cl.
CPC ...
C07F 7/2212 (2013.01); C07C 1/325 (2013.01); C07C 17/093 (2013.01); C07C 29/42 (2013.01); C07C 41/01 (2013.01); C07C 41/16 (2013.01); C07C 41/30 (2013.01); C07C 45/00 (2013.01); C07C 67/333 (2013.01); C07C 253/30 (2013.01); C07D 213/16 (2013.01); C07D 239/26 (2013.01); C07D 333/08 (2013.01); C07C 2103/10 (2013.01);
Abstract

Disclosed are methods for rerouting radical cascade cyclizations by using alkenes as alkyne equivalents. The reaction sequence is initiated by a novel 1,2 stannyl shift which achieves chemo- and regioselectivity in the process. The radical 'hopping' leads to the formation of the radical center necessary for the sequence of selective cyclizations and fragmentations to follow. In the last step of the cascade, the elimination of a rationally designed radical leaving group via β-C—C bond scission aromatizes the product without the need for external oxidant. The BuSn moiety, which is installed during the reaction sequence, allows further functionalization of the product via facile reactions with electrophiles as well as Stille and Suzuki cross-coupling reactions. This selective radical transformation opens a new approach for the controlled transformation of enynes into extended polycyclic structures of tunable dimensions.


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