Improved, stereospecific synthesis of highly substituted butyrolactones via dyotropic rearrangement

T. Howard Black; Jeffrey A. Hall; Robert G. Sheu

doi:10.1021/jo00245a050

Improved, stereospecific synthesis of highly substituted butyrolactones via dyotropic rearrangement

The Journal of Organic Chemistry ◽

10.1021/jo00245a050 ◽

1988 ◽

Vol 53 (10) ◽

pp. 2371-2374 ◽

Cited By ~ 36

Author(s):

T. Howard Black ◽

Jeffrey A. Hall ◽

Robert G. Sheu

Keyword(s):

Stereospecific Synthesis ◽

Dyotropic Rearrangement

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ChemInform Abstract: Improved, Stereospecific Synthesis of Highly Substituted Butyrolactones via Dyotropic Rearrangement.

ChemInform ◽

10.1002/chin.198842186 ◽

1988 ◽

Vol 19 (42) ◽

Author(s):

T. H. BLACK ◽

J. A. HALL ◽

R. G. SHEU

Keyword(s):

Stereospecific Synthesis ◽

Dyotropic Rearrangement

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Stereospecific synthesis of 11Z-hexadedenal – the main component of the sex pheromone of Helicoverpa armigera Hbn. from the cyclodimer of butadiene and isoprene

PROCEEDINGS OF IV INTERNATIONAL SCIENTIFIC CONFERENCE “CURRENT STATE, PROBLEMS AND PROSPECTS OF THE DEVELOPMENT OF AGRARIAN SCIENCE” ◽

10.33952/09.09.2019.174 ◽

2019 ◽

Author(s):

G.Yu. Ishmuratov ◽

◽

Yu.V. Myasoedova ◽

L.R. Garifullina ◽

E.R. Nurieva ◽

...

Keyword(s):

Sex Pheromone ◽

Helicoverpa Armigera ◽

Stereospecific Synthesis ◽

Helicoverpa Armígera ◽

Main Component

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Faculty Opinions recommendation of Direct stereospecific synthesis of unprotected N-H and N-Me aziridines from olefins.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.718226654.793490007 ◽

2014 ◽

Author(s):

Roger Freidinger

Keyword(s):

Stereospecific Synthesis

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Stereospecific Synthesis of m-Hydroxymexiletine Enantiomers

Drug Metabolism Letters ◽

10.2174/1872312811206030005 ◽

2013 ◽

Vol 6 (3) ◽

pp. 182-186 ◽

Cited By ~ 6

Author(s):

Alessia Catalano ◽

Alessia Carocci ◽

Giovanni Lentini ◽

Ivana Defrenza ◽

Claudio Bruno ◽

...

Keyword(s):

Stereospecific Synthesis

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Stereospecific synthesis of functionalized cyclopentanes

Tetrahedron Letters ◽

10.1016/s0040-4039(00)76202-2 ◽

1989 ◽

Vol 30 (42) ◽

pp. 5803-5806 ◽

Cited By ~ 26

Author(s):

Alfred Hassner ◽

Rakesh Maurya

Keyword(s):

Stereospecific Synthesis

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ChemInform Abstract: An Efficient, Stereospecific Synthesis of the Dimer-Selective Retinoid X Receptor Modulator (2E,4E,6Z)-7- [5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-(n-propyloxy)naphthalen-3-yl] -3-methylocta-2,4,6-trienoic Acid.

ChemInform ◽

10.1002/chin.200036098 ◽

2010 ◽

Vol 31 (36) ◽

pp. no-no

Author(s):

Lawrence G. Hamann

Keyword(s):

Retinoid X Receptor ◽

Trienoic Acid ◽

Stereospecific Synthesis ◽

Receptor Modulator

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Stereospecific Synthesis of Pyrene-Fused [5]Helicenes

Synfacts ◽

10.1055/s-0040-1719766 ◽

2021 ◽

Vol 17 (04) ◽

pp. 0390

Keyword(s):

Stereospecific Synthesis

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ChemInform Abstract: TOTAL STEREOSPECIFIC SYNTHESIS OF CIS-CHRYSANTHEMIC METHYL ESTER: THE CYCLOPROPENIC WAY

Chemischer Informationsdienst ◽

10.1002/chin.198022144 ◽

1980 ◽

Vol 11 (22) ◽

Author(s):

M. FRANCK-NEUMANN ◽

C. DIETRICH-BUCHECKER

Keyword(s):

Methyl Ester ◽

Stereospecific Synthesis

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ChemInform Abstract: STEREOSPECIFIC SYNTHESIS OF A 3-PHENYLISOCHROMAN-1-ONE

Chemischer Informationsdienst ◽

10.1002/chin.197847192 ◽

1978 ◽

Vol 9 (47) ◽

Author(s):

W. WIEGREBE ◽

S. PRIOR

Keyword(s):

Stereospecific Synthesis

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C–C bond activation enabled by dyotropic rearrangement of Pd(iv) species

Nature Chemistry ◽

10.1038/s41557-021-00698-y ◽

2021 ◽

Author(s):

Jian Cao ◽

Hua Wu ◽

Qian Wang ◽

Jieping Zhu

Keyword(s):

Bond Activation ◽

Dyotropic Rearrangement

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