Organic and Biomolecular Chemistry

, том 12 , издание 32 , страницы 6121-6127

Total synthesis of fluoxetine and duloxetine through an in situ imine formation/borylation/transimination and reduction approach

Тип публикации: Journal Article

Дата публикации: 2014-07-03

Royal Society of Chemistry (RSC)

Organic and Biomolecular Chemistry

SCImago Q2

WOS Q2

БС1

SJR: 0.475

CiteScore: 4.8

Impact factor: 2.8

ISSN: 14770520, 14770539

DOI: 10.1039/c4ob01142b

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PubMed ID: 25004984

Organic Chemistry

Biochemistry

Physical and Theoretical Chemistry

Краткое описание

Efficient, catalytic, asymmetric total syntheses of both (R)-fluoxetine and (S)-duloxetine from α,β-unsaturated aldehydes are reported.

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Calow A. D. J., Fernández E., Redfern C. Total synthesis of fluoxetine and duloxetine through an in situ imine formation/borylation/transimination and reduction approach // Organic and Biomolecular Chemistry. 2014. Vol. 12. No. 32. pp. 6121-6127.

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TY - JOUR

DO - 10.1039/c4ob01142b

UR - https://doi.org/10.1039/c4ob01142b

TI - Total synthesis of fluoxetine and duloxetine through an in situ imine formation/borylation/transimination and reduction approach

T2 - Organic and Biomolecular Chemistry

AU - Calow, Adam D J

AU - Fernández, Elena

AU - Redfern, Chris

PY - 2014

DA - 2014/07/03

PB - Royal Society of Chemistry (RSC)

SP - 6121-6127

IS - 32

VL - 12

PMID - 25004984

SN - 1477-0520

SN - 1477-0539

ER -

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@article{2014_Calow,

author = {Adam D J Calow and Elena Fernández and Chris Redfern},

title = {Total synthesis of fluoxetine and duloxetine through an in situ imine formation/borylation/transimination and reduction approach},

journal = {Organic and Biomolecular Chemistry},

year = {2014},

volume = {12},

publisher = {Royal Society of Chemistry (RSC)},

month = {jul},

url = {https://doi.org/10.1039/c4ob01142b},

number = {32},

pages = {6121--6127},

doi = {10.1039/c4ob01142b}

}

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Calow, Adam D. J., et al. “Total synthesis of fluoxetine and duloxetine through an in situ imine formation/borylation/transimination and reduction approach.” Organic and Biomolecular Chemistry, vol. 12, no. 32, Jul. 2014, pp. 6121-6127. https://doi.org/10.1039/c4ob01142b.

Издатель

Royal Society of Chemistry (RSC)

Журнал

Organic and Biomolecular Chemistry

SCImago Q2

WOS Q2

БС1

SJR

0.475

CiteScore

4.8

Impact factor