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Reactions of Alkenes: The Usami Synthesis of (−)-Pericosine E

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Dasheng Leow of the National Tsing Hua University used (Eur. J. Org. Chem. 2014, 7347) photolysis to activate the air oxidation of hydrazine to generate diimide, that then reduced 1 selectively to 2. Kevin M. Peese of Bristol-Myers Squibb effected (Org. Lett. 2014, 16, 4444) ring-closing metathesis of 3 followed by in situ reduction to form 4. Jitendra K. Bera of the Indian Institute of Technology Kanpur effected (J. Am. Chem. Soc. 2014, 136, 13987) gentle oxidative cleavage of cyclooctene 5 to the dialde­hyde 6. Arumugam Sudalai of the National Chemical Laboratory observed (Org. Lett. 2014, 16, 5674) high regioselectivity in the oxidation of the alkene 7 to the ketone 8. Hao Xu of Georgia State University also observed (J. Am. Chem. Soc. 2014, 136, 13186) high regioselectivity in the oxidation of the alkene 9 with 10, leading to the urethane 11. Justin Du Bois of Stanford University developed (J. Am. Chem. Soc. 2014, 136, 13506) mild conditions for the net double amination of the alkene 12 with 13, leading to 14. Jiaxi Xu and Pingfan Li of the Beijing University of Chemical Technology devised (Org. Lett. 2014, 16, 6036) a protocol for the allylic thiomethylation of an alkene with 16, converting 15 to 17. Matthias Beller of the Leibniz-Institüt für Katalyse combined (Chem. Eur. J. 2014, 20, 15692) hydroformylation, aldol condensation, and reduction to convert the alkene 18 to the ketone 19. Phil S. Baran of Scripps/La Jolla added (Angew. Chem. Int. Ed. 2014, 53, 14382) the diazo dienone 21 to the alkene 20 to give, after exposure to HCl, the arylated product 22. Markus R. Heinrich of the Friedrich-Alexander-Universität Erlangen-Nürnberg employed (Chem. Eur. J. 2014, 20, 15344) Selectfluor as both an oxidizing and a fluorinating agent in the related addition of 24 to 23 to give 25. Debabrata Maiti at the Indian Institute of Technology Bombay activated (J. Am. Chem. Soc. 2014, 136, 13602) the ortho position of 27, then added that interme­diate to 26 to give 28.
Oxford University Press
Title: Reactions of Alkenes: The Usami Synthesis of (−)-Pericosine E
Description:
Dasheng Leow of the National Tsing Hua University used (Eur.
J.
Org.
Chem.
2014, 7347) photolysis to activate the air oxidation of hydrazine to generate diimide, that then reduced 1 selectively to 2.
Kevin M.
Peese of Bristol-Myers Squibb effected (Org.
Lett.
2014, 16, 4444) ring-closing metathesis of 3 followed by in situ reduction to form 4.
Jitendra K.
Bera of the Indian Institute of Technology Kanpur effected (J.
Am.
Chem.
Soc.
2014, 136, 13987) gentle oxidative cleavage of cyclooctene 5 to the dialde­hyde 6.
Arumugam Sudalai of the National Chemical Laboratory observed (Org.
Lett.
2014, 16, 5674) high regioselectivity in the oxidation of the alkene 7 to the ketone 8.
Hao Xu of Georgia State University also observed (J.
Am.
Chem.
Soc.
2014, 136, 13186) high regioselectivity in the oxidation of the alkene 9 with 10, leading to the urethane 11.
Justin Du Bois of Stanford University developed (J.
Am.
Chem.
Soc.
2014, 136, 13506) mild conditions for the net double amination of the alkene 12 with 13, leading to 14.
Jiaxi Xu and Pingfan Li of the Beijing University of Chemical Technology devised (Org.
Lett.
2014, 16, 6036) a protocol for the allylic thiomethylation of an alkene with 16, converting 15 to 17.
Matthias Beller of the Leibniz-Institüt für Katalyse combined (Chem.
Eur.
J.
2014, 20, 15692) hydroformylation, aldol condensation, and reduction to convert the alkene 18 to the ketone 19.
Phil S.
Baran of Scripps/La Jolla added (Angew.
Chem.
Int.
Ed.
2014, 53, 14382) the diazo dienone 21 to the alkene 20 to give, after exposure to HCl, the arylated product 22.
Markus R.
Heinrich of the Friedrich-Alexander-Universität Erlangen-Nürnberg employed (Chem.
Eur.
J.
2014, 20, 15344) Selectfluor as both an oxidizing and a fluorinating agent in the related addition of 24 to 23 to give 25.
Debabrata Maiti at the Indian Institute of Technology Bombay activated (J.
Am.
Chem.
Soc.
2014, 136, 13602) the ortho position of 27, then added that interme­diate to 26 to give 28.

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