Olefinazione di Peterson (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Olefinazione di Peterson" in Italian language version.

refsWebsite

Global rank Italian rank

15doi.org

2^nd place

7^th place

5oadoi.org

799^th place

22^nd place

2nih.gov

4^th place

9^th place

1orgsyn.org

2,971^st place

5,289^th place

1organic-chemistry.org

low place

doi.org

dx.doi.org

D. J. Peterson, Carbonyl olefination reaction using silyl-substituted organometallic compounds, in J. Org. Chem., vol. 33, n. 2, 1968, pp. 780–784, DOI:10.1021/jo01266a061.
Ager, D. J. Org. React. 1990, 38, 1. DOI: 10.1002/0471264180.or038.01
T. H. Chan, Alkene synthesis via β-functionalized organosilicon compounds, in Accounts of Chemical Research, vol. 10, n. 12, 1977, pp. 442–448, DOI:10.1021/ar50120a003.
New developments in the Peterson olefination reaction L. Frances van Staden, David Gravestock and David J. Ager Chem. Soc. Rev., 2002,31, 195-200 DOI: 10.1039/A908402I
Manas Das e Donal F. O’Shea, Z-Stereoselective Aza-Peterson Olefinations with Bis(trimethylsilane) Reagents and Sulfinyl Imines, in Organic Letters, vol. 18, n. 2, 15 gennaio 2016, pp. 336–339, DOI:10.1021/acs.orglett.5b03519. URL consultato il 6 gennaio 2022.
Thomas K. Britten e Mark G. McLaughlin, Brønsted Acid Catalyzed Peterson Olefinations, in The Journal of Organic Chemistry, vol. 85, n. 2, 17 gennaio 2020, pp. 301–305, DOI:10.1021/acs.joc.9b02489. URL consultato il 6 gennaio 2022.
Wanxiang Zhao e Jianwei Sun, Triflimide (HNTf2) in Organic Synthesis, in Chemical Reviews, vol. 118, n. 20, 24 ottobre 2018, pp. 10349–10392, DOI:10.1021/acs.chemrev.8b00279. URL consultato il 6 gennaio 2022.
Kaori Ando, Tomohiro Wada e Miho Okumura, Stereoselective Synthesis of Z-α,β-Unsaturated Sulfones Using Peterson Reagents, in Organic Letters, vol. 17, n. 24, 18 dicembre 2015, pp. 6026–6029, DOI:10.1021/acs.orglett.5b03008. URL consultato il 6 gennaio 2022.
T. H. Chan e E. Chang, Synthesis of alkenes from carbonyl compounds and carbanions alpha to silicon. III. Full report and a synthesis of the sex pheromone of gypsy moth, in J. Org. Chem., vol. 39, n. 22, 1974, pp. 3264–3268, DOI:10.1021/jo00936a020, PMID 4473100.
X. Zeng, F. Zeng e E. Negishi, Efficient and Selective Synthesis of 6,7-Dehydrostipiamide via Zr-Catalyzed Asymmetric Carboalumination and Pd-Catalyzed Cross-Coupling of Organozincs, in Org. Lett., vol. 6, n. 19, 2004, pp. 3245–3248, DOI:10.1021/ol048905v, PMID 15355023.
E. J. Corey, D. Enders e M. G. Bock, A simple and highly effective route to α-β-unsaturated aldehydes, in Tetrahedron Letters, vol. 17, n. 1, 1976, pp. 7–10, DOI:10.1016/S0040-4039(00)71308-6.

doi.org

Manas Das e Donal F. O’Shea, Z-Stereoselective Aza-Peterson Olefinations with Bis(trimethylsilane) Reagents and Sulfinyl Imines, in Organic Letters, vol. 18, n. 2, 15 gennaio 2016, pp. 336–339, DOI:10.1021/acs.orglett.5b03519. URL consultato il 6 gennaio 2022.
Thomas K. Britten e Mark G. McLaughlin, Brønsted Acid Catalyzed Peterson Olefinations, in The Journal of Organic Chemistry, vol. 85, n. 2, 17 gennaio 2020, pp. 301–305, DOI:10.1021/acs.joc.9b02489. URL consultato il 6 gennaio 2022.
Wanxiang Zhao e Jianwei Sun, Triflimide (HNTf2) in Organic Synthesis, in Chemical Reviews, vol. 118, n. 20, 24 ottobre 2018, pp. 10349–10392, DOI:10.1021/acs.chemrev.8b00279. URL consultato il 6 gennaio 2022.
Kaori Ando, Tomohiro Wada e Miho Okumura, Stereoselective Synthesis of Z-α,β-Unsaturated Sulfones Using Peterson Reagents, in Organic Letters, vol. 17, n. 24, 18 dicembre 2015, pp. 6026–6029, DOI:10.1021/acs.orglett.5b03008. URL consultato il 6 gennaio 2022.

nih.gov

ncbi.nlm.nih.gov

T. H. Chan e E. Chang, Synthesis of alkenes from carbonyl compounds and carbanions alpha to silicon. III. Full report and a synthesis of the sex pheromone of gypsy moth, in J. Org. Chem., vol. 39, n. 22, 1974, pp. 3264–3268, DOI:10.1021/jo00936a020, PMID 4473100.
X. Zeng, F. Zeng e E. Negishi, Efficient and Selective Synthesis of 6,7-Dehydrostipiamide via Zr-Catalyzed Asymmetric Carboalumination and Pd-Catalyzed Cross-Coupling of Organozincs, in Org. Lett., vol. 6, n. 19, 2004, pp. 3245–3248, DOI:10.1021/ol048905v, PMID 15355023.

oadoi.org

D. J. Peterson, Carbonyl olefination reaction using silyl-substituted organometallic compounds, in J. Org. Chem., vol. 33, n. 2, 1968, pp. 780–784, DOI:10.1021/jo01266a061.
T. H. Chan, Alkene synthesis via β-functionalized organosilicon compounds, in Accounts of Chemical Research, vol. 10, n. 12, 1977, pp. 442–448, DOI:10.1021/ar50120a003.
T. H. Chan e E. Chang, Synthesis of alkenes from carbonyl compounds and carbanions alpha to silicon. III. Full report and a synthesis of the sex pheromone of gypsy moth, in J. Org. Chem., vol. 39, n. 22, 1974, pp. 3264–3268, DOI:10.1021/jo00936a020, PMID 4473100.
X. Zeng, F. Zeng e E. Negishi, Efficient and Selective Synthesis of 6,7-Dehydrostipiamide via Zr-Catalyzed Asymmetric Carboalumination and Pd-Catalyzed Cross-Coupling of Organozincs, in Org. Lett., vol. 6, n. 19, 2004, pp. 3245–3248, DOI:10.1021/ol048905v, PMID 15355023.
E. J. Corey, D. Enders e M. G. Bock, A simple and highly effective route to α-β-unsaturated aldehydes, in Tetrahedron Letters, vol. 17, n. 1, 1976, pp. 7–10, DOI:10.1016/S0040-4039(00)71308-6.

organic-chemistry.org

Peterson Olefination, su www.organic-chemistry.org. URL consultato il 6 gennaio 2022.

orgsyn.org

(EN) Organic Syntheses, http://www.orgsyn.org/demo.aspx?prep=cv9p0580 Titolo mancante per url url (aiuto).