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Hydroxylamine as an ammonia equivalent: access to NH-tetrahydroisoquinolonic derivatives from aldoximes by the Castagnoli–Cushman reaction followed by reduction. / Bannykh, Anton V.; Bakulina, Olga Yu; Dar'in, Dmitry V.; Krasavin, Mikhail.

In: Mendeleev Communications , Vol. 29, No. 3, 01.05.2019, p. 337-338.

Research output: Contribution to journal › Article › peer-review

Harvard

Bannykh, AV, Bakulina, OY, Dar'in, DV & Krasavin, M 2019, 'Hydroxylamine as an ammonia equivalent: access to NH-tetrahydroisoquinolonic derivatives from aldoximes by the Castagnoli–Cushman reaction followed by reduction', Mendeleev Communications , vol. 29, no. 3, pp. 337-338. https://doi.org/10.1016/j.mencom.2019.05.033

APA

Bannykh, A. V., Bakulina, O. Y., Dar'in, D. V., & Krasavin, M. (2019). Hydroxylamine as an ammonia equivalent: access to NH-tetrahydroisoquinolonic derivatives from aldoximes by the Castagnoli–Cushman reaction followed by reduction. Mendeleev Communications , 29(3), 337-338. https://doi.org/10.1016/j.mencom.2019.05.033

Vancouver

Bannykh AV, Bakulina OY, Dar'in DV, Krasavin M. Hydroxylamine as an ammonia equivalent: access to NH-tetrahydroisoquinolonic derivatives from aldoximes by the Castagnoli–Cushman reaction followed by reduction. Mendeleev Communications . 2019 May 1;29(3):337-338. https://doi.org/10.1016/j.mencom.2019.05.033

Author

Bannykh, Anton V. ; Bakulina, Olga Yu ; Dar'in, Dmitry V. ; Krasavin, Mikhail. / Hydroxylamine as an ammonia equivalent: access to NH-tetrahydroisoquinolonic derivatives from aldoximes by the Castagnoli–Cushman reaction followed by reduction. In: Mendeleev Communications . 2019 ; Vol. 29, No. 3. pp. 337-338.

BibTeX

@article{096bb9d8faa54db285be1739147c23b8,
title = "Hydroxylamine as an ammonia equivalent: access to NH-tetrahydroisoquinolonic derivatives from aldoximes by the Castagnoli–Cushman reaction followed by reduction",
abstract = "A novel synthetic protocol towards trans-NH-tetrahydroisoquinolonic acid esters is based on the Castagnoli–Cushman reaction between aromatic aldehyde oximes and homophthalic anhydride, followed by esterification and TiCl3-promoted reduction. The scope of the method with respect to the aromatic portion (both electron-rich and electron-deficient) is broader compared to the earlier described approaches, which makes it a suitable synthetic strategy for the structure–activity exploration.",
keywords = "CYCLOADDITION",
author = "Bannykh, {Anton V.} and Bakulina, {Olga Yu} and Dar'in, {Dmitry V.} and Mikhail Krasavin",
year = "2019",
month = may,
day = "1",
doi = "10.1016/j.mencom.2019.05.033",
language = "English",
volume = "29",
pages = "337--338",
journal = "Mendeleev Communications",
issn = "0959-9436",
publisher = "Elsevier",
number = "3",

}

RIS

TY - JOUR

T1 - Hydroxylamine as an ammonia equivalent: access to NH-tetrahydroisoquinolonic derivatives from aldoximes by the Castagnoli–Cushman reaction followed by reduction

AU - Bannykh, Anton V.

AU - Bakulina, Olga Yu

AU - Dar'in, Dmitry V.

AU - Krasavin, Mikhail

PY - 2019/5/1

Y1 - 2019/5/1

N2 - A novel synthetic protocol towards trans-NH-tetrahydroisoquinolonic acid esters is based on the Castagnoli–Cushman reaction between aromatic aldehyde oximes and homophthalic anhydride, followed by esterification and TiCl3-promoted reduction. The scope of the method with respect to the aromatic portion (both electron-rich and electron-deficient) is broader compared to the earlier described approaches, which makes it a suitable synthetic strategy for the structure–activity exploration.

AB - A novel synthetic protocol towards trans-NH-tetrahydroisoquinolonic acid esters is based on the Castagnoli–Cushman reaction between aromatic aldehyde oximes and homophthalic anhydride, followed by esterification and TiCl3-promoted reduction. The scope of the method with respect to the aromatic portion (both electron-rich and electron-deficient) is broader compared to the earlier described approaches, which makes it a suitable synthetic strategy for the structure–activity exploration.

KW - CYCLOADDITION

UR - http://www.scopus.com/inward/record.url?scp=85066877174&partnerID=8YFLogxK

UR - http://www.mendeley.com/research/hydroxylamine-ammonia-equivalent-access-nhtetrahydroisoquinolonic-derivatives-aldoximes-castagnolicu

U2 - 10.1016/j.mencom.2019.05.033

DO - 10.1016/j.mencom.2019.05.033

M3 - Article

AN - SCOPUS:85066877174

VL - 29

SP - 337

EP - 338

JO - Mendeleev Communications

JF - Mendeleev Communications

SN - 0959-9436

IS - 3

ER -

ID: 46204154