Tetrahedron Letters

, том 45 , издание 4 , страницы 739-742

Novel 3′-deoxy analogs of the anti-HBV agent entecavir: synthesis of enantiomers from a single chiral epoxide

Тип публикации: Journal Article

Дата публикации: 2004-01-01

Elsevier

Tetrahedron Letters

scimago Q3

wos Q3

БС2

SJR: 0.334

CiteScore: 3.2

Impact factor: 1.5

ISSN: 00404039, 18733581

DOI: 10.1016/j.tetlet.2003.11.052

Скопировать DOI

Organic Chemistry

Drug Discovery

Biochemistry

Краткое описание

A synthesis of novel 3′-deoxy analogs of the anti-HBV agent entecavir (BMS-200475) was devised using regioselective ring opening of suitable cyclopentene epoxides as the key step. This versatile approach afforded access to an enantiomeric pair of carbocyclic nucleosides from a single chiral intermediate.

Найдено

Для доступа к списку цитирований публикации необходимо авторизоваться.

Войти с ORCID

Для доступа к списку профилей, цитирующих публикацию, необходимо авторизоваться.

Войти с ORCID

Топ-30

Журналы

	1 2 3 4
Tetrahedron Letters	Tetrahedron Letters, 4, 10.26% Tetrahedron Letters 4 публикации, 10.26%
Journal of Organic Chemistry	Journal of Organic Chemistry, 4, 10.26% Journal of Organic Chemistry 4 публикации, 10.26%
Synlett	Synlett, 3, 7.69% Synlett 3 публикации, 7.69%
Mendeleev Communications	Mendeleev Communications, 2, 5.13% Mendeleev Communications 2 публикации, 5.13%
Industrial & Engineering Chemistry Research	Industrial & Engineering Chemistry Research, 2, 5.13% Industrial & Engineering Chemistry Research 2 публикации, 5.13%
Synthesis	Synthesis, 2, 5.13% Synthesis 2 публикации, 5.13%
Research on Chemical Intermediates	Research on Chemical Intermediates, 1, 2.56% Research on Chemical Intermediates 1 публикация, 2.56%
Journal of Fuel Chemistry and Technology	Journal of Fuel Chemistry and Technology, 1, 2.56% Journal of Fuel Chemistry and Technology 1 публикация, 2.56%
Journal of Organometallic Chemistry	Journal of Organometallic Chemistry, 1, 2.56% Journal of Organometallic Chemistry 1 публикация, 2.56%
Polymer	Polymer, 1, 2.56% Polymer 1 публикация, 2.56%
Inorganic Chemistry Communication	Inorganic Chemistry Communication, 1, 2.56% Inorganic Chemistry Communication 1 публикация, 2.56%
Polyhedron	Polyhedron, 1, 2.56% Polyhedron 1 публикация, 2.56%
Tetrahedron Asymmetry	Tetrahedron Asymmetry, 1, 2.56% Tetrahedron Asymmetry 1 публикация, 2.56%
Tetrahedron	Tetrahedron, 1, 2.56% Tetrahedron 1 публикация, 2.56%
Applied Catalysis A: General	Applied Catalysis A: General, 1, 2.56% Applied Catalysis A: General 1 публикация, 2.56%
Comptes Rendus Chimie	Comptes Rendus Chimie, 1, 2.56% Comptes Rendus Chimie 1 публикация, 2.56%
ChemInform	ChemInform, 1, 2.56% ChemInform 1 публикация, 2.56%
Chemistry - An Asian Journal	Chemistry - An Asian Journal, 1, 2.56% Chemistry - An Asian Journal 1 публикация, 2.56%
ChemSusChem	ChemSusChem, 1, 2.56% ChemSusChem 1 публикация, 2.56%
Expert Review of Anti-Infective Therapy	Expert Review of Anti-Infective Therapy, 1, 2.56% Expert Review of Anti-Infective Therapy 1 публикация, 2.56%
Synthesis and Reactivity in Inorganic Metal-Organic and Nano-Metal Chemistry	Synthesis and Reactivity in Inorganic Metal-Organic and Nano-Metal Chemistry, 1, 2.56% Synthesis and Reactivity in Inorganic Metal-Organic and Nano-Metal Chemistry 1 публикация, 2.56%
Polymers	Polymers, 1, 2.56% Polymers 1 публикация, 2.56%
	1 2 3 4

Издатели

	2 4 6 8 10 12 14 16
Elsevier	Elsevier, 16, 41.03% Elsevier 16 публикаций, 41.03%
American Chemical Society (ACS)	American Chemical Society (ACS), 6, 15.38% American Chemical Society (ACS) 6 публикаций, 15.38%
Wiley	Wiley, 5, 12.82% Wiley 5 публикаций, 12.82%
Georg Thieme Verlag KG	Georg Thieme Verlag KG, 5, 12.82% Georg Thieme Verlag KG 5 публикаций, 12.82%
Taylor & Francis	Taylor & Francis, 2, 5.13% Taylor & Francis 2 публикации, 5.13%
Springer Nature	Springer Nature, 1, 2.56% Springer Nature 1 публикация, 2.56%
MDPI	MDPI, 1, 2.56% MDPI 1 публикация, 2.56%
	2 4 6 8 10 12 14 16

Мы не учитываем публикации, у которых нет DOI.
Статистика публикаций обновляется еженедельно.

Вы ученый?

Создайте профиль, чтобы получать персональные рекомендации коллег, конференций и новых статей.

Войти с ORCID

Метрики

Цитировать

ГОСТ |

Цитировать

ГОСТ Скопировать

Ruediger E. et al. Novel 3′-deoxy analogs of the anti-HBV agent entecavir: synthesis of enantiomers from a single chiral epoxide // Tetrahedron Letters. 2004. Vol. 45. No. 4. pp. 739-742.

ГОСТ со всеми авторами (до 50) Скопировать

Ruediger E., Martel A. Y., Meanwell N. A., Solomon C., Turmel B. Novel 3′-deoxy analogs of the anti-HBV agent entecavir: synthesis of enantiomers from a single chiral epoxide // Tetrahedron Letters. 2004. Vol. 45. No. 4. pp. 739-742.

RIS |

Цитировать

RIS Скопировать

TY - JOUR

DO - 10.1016/j.tetlet.2003.11.052

UR - https://doi.org/10.1016/j.tetlet.2003.11.052

TI - Novel 3′-deoxy analogs of the anti-HBV agent entecavir: synthesis of enantiomers from a single chiral epoxide

T2 - Tetrahedron Letters

AU - Ruediger, Edward

AU - Martel, Alain Y.

AU - Meanwell, Nicholas A.

AU - Solomon, Carola

AU - Turmel, Brigitte

PY - 2004

DA - 2004/01/01

PB - Elsevier

SP - 739-742

IS - 4

VL - 45

SN - 0040-4039

SN - 1873-3581

ER -

BibTex |

Цитировать

BibTex (до 50 авторов) Скопировать

@article{2004_Ruediger,

author = {Edward Ruediger and Alain Y. Martel and Nicholas A. Meanwell and Carola Solomon and Brigitte Turmel},

title = {Novel 3′-deoxy analogs of the anti-HBV agent entecavir: synthesis of enantiomers from a single chiral epoxide},

journal = {Tetrahedron Letters},

year = {2004},

volume = {45},

publisher = {Elsevier},

month = {jan},

url = {https://doi.org/10.1016/j.tetlet.2003.11.052},

number = {4},

pages = {739--742},

doi = {10.1016/j.tetlet.2003.11.052}

}

MLA

Цитировать

MLA Скопировать

Ruediger, Edward, et al. “Novel 3′-deoxy analogs of the anti-HBV agent entecavir: synthesis of enantiomers from a single chiral epoxide.” Tetrahedron Letters, vol. 45, no. 4, Jan. 2004, pp. 739-742. https://doi.org/10.1016/j.tetlet.2003.11.052.

Издатель

Elsevier

Журнал

Tetrahedron Letters

scimago Q3

wos Q3

БС2

SJR

0.334

CiteScore

3.2

Impact factor

1.5

ISSN

00404039 (Print)

18733581 (Electronic)