Standard

A Route to Benzo-Annelated δ-Sultams through Michael Cyclization. / Соколов, Виктор Владимирович; Рассадин, Валентин Анатольевич; Grosheva, Daria S.

In: European Journal of Organic Chemistry, Vol. 6, No. 6, 2015, p. 1355-1363.

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

Harvard

Соколов, ВВ, Рассадин, ВА & Grosheva, DS 2015, 'A Route to Benzo-Annelated δ-Sultams through Michael Cyclization', European Journal of Organic Chemistry, vol. 6, no. 6, pp. 1355-1363. https://doi.org/10.1002/ejoc.201403416, https://doi.org/10.1002/ejoc.201403416

APA

Соколов, В. В., Рассадин, В. А., & Grosheva, D. S. (2015). A Route to Benzo-Annelated δ-Sultams through Michael Cyclization. European Journal of Organic Chemistry, 6(6), 1355-1363. https://doi.org/10.1002/ejoc.201403416, https://doi.org/10.1002/ejoc.201403416

Vancouver

Соколов ВВ, Рассадин ВА, Grosheva DS. A Route to Benzo-Annelated δ-Sultams through Michael Cyclization. European Journal of Organic Chemistry. 2015;6(6):1355-1363. https://doi.org/10.1002/ejoc.201403416, https://doi.org/10.1002/ejoc.201403416

Author

Соколов, Виктор Владимирович ; Рассадин, Валентин Анатольевич ; Grosheva, Daria S. / A Route to Benzo-Annelated δ-Sultams through Michael Cyclization. In: European Journal of Organic Chemistry. 2015 ; Vol. 6, No. 6. pp. 1355-1363.

BibTeX

@article{a2e092ed757b4d35be9395af575efee2,
title = "A Route to Benzo-Annelated δ-Sultams through Michael Cyclization",
abstract = "A new approach to benzo-annelated δ-sultams containing anaryl–nitrogen bond is described. The method, which involvesthe intramolecular Michael cyclization of tert-butyl ortho-[N-(methoxycarbonylmethyl)sulfonylamino]cinnamates, allows the synthesis of secondary sultams as well as their tertiaryanalogues and bridged tricyclic derivatives efficiently anddiastereoselectively.",
keywords = "Heterocycles / Sultams / Fused-ring systems / Michael addition / Cyclization",
author = "Соколов, {Виктор Владимирович} and Рассадин, {Валентин Анатольевич} and Grosheva, {Daria S.}",
year = "2015",
doi = "10.1002/ejoc.201403416",
language = "English",
volume = "6",
pages = "1355--1363",
journal = "European Journal of Organic Chemistry",
issn = "1434-193X",
publisher = "Wiley-Blackwell",
number = "6",

}

RIS

TY - JOUR

T1 - A Route to Benzo-Annelated δ-Sultams through Michael Cyclization

AU - Соколов, Виктор Владимирович

AU - Рассадин, Валентин Анатольевич

AU - Grosheva, Daria S.

PY - 2015

Y1 - 2015

N2 - A new approach to benzo-annelated δ-sultams containing anaryl–nitrogen bond is described. The method, which involvesthe intramolecular Michael cyclization of tert-butyl ortho-[N-(methoxycarbonylmethyl)sulfonylamino]cinnamates, allows the synthesis of secondary sultams as well as their tertiaryanalogues and bridged tricyclic derivatives efficiently anddiastereoselectively.

AB - A new approach to benzo-annelated δ-sultams containing anaryl–nitrogen bond is described. The method, which involvesthe intramolecular Michael cyclization of tert-butyl ortho-[N-(methoxycarbonylmethyl)sulfonylamino]cinnamates, allows the synthesis of secondary sultams as well as their tertiaryanalogues and bridged tricyclic derivatives efficiently anddiastereoselectively.

KW - Heterocycles / Sultams / Fused-ring systems / Michael addition / Cyclization

U2 - 10.1002/ejoc.201403416

DO - 10.1002/ejoc.201403416

M3 - Article

VL - 6

SP - 1355

EP - 1363

JO - European Journal of Organic Chemistry

JF - European Journal of Organic Chemistry

SN - 1434-193X

IS - 6

ER -

ID: 3927987