Home / Publications / Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects

Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects

Lidia Sergeevna Konstantinova 1
Lidia Sergeevna Konstantinova
, 
Oleg Alexeevich Rakitin 1
Oleg Alexeevich Rakitin
10.1016/j.mencom.2009.03.001
Published 2009-03-10
Focus article , Volume 19, Issue 2, 55-61
21
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Konstantinova L. S., Rakitin O. A. Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects // Mendeleev Communications. 2009. Vol. 19. No. 2. pp. 55-61.
GOST all authors (up to 50) Copy
Konstantinova L. S., Rakitin O. A. Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects // Mendeleev Communications. 2009. Vol. 19. No. 2. pp. 55-61.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2009.03.001
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.03.001
TI - Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects
T2 - Mendeleev Communications
AU - Konstantinova, Lidia Sergeevna
AU - Rakitin, Oleg Alexeevich
PY - 2009
DA - 2009/03/10
PB - Mendeleev Communications
SP - 55-61
IS - 2
VL - 19
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2009_Konstantinova,
author = {Lidia Sergeevna Konstantinova and Oleg Alexeevich Rakitin},
title = {Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects},
journal = {Mendeleev Communications},
year = {2009},
volume = {19},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.03.001},
number = {2},
pages = {55--61},
doi = {10.1016/j.mencom.2009.03.001}
}
MLA
Cite this
MLA Copy
Konstantinova, Lidia Sergeevna, and Oleg Alexeevich Rakitin. “Design of sulfur heterocycles with sulfur monochloride: synthetic possibilities and prospects.” Mendeleev Communications, vol. 19, no. 2, Mar. 2009, pp. 55-61. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.03.001.
Views / Downloads
1 / 2

Abstract

Sulfur monochloride is an important reagent in the synthesis of heterocycles with various numbers of sulfur atoms. The classification is proposed for the selective synthesis of highly interesting sulfur heterocyclic systems from acyclic fragments containing C–H, CN, C≡N and C–Cl bonds.

References

1.
Chapter 4 Sulfur Monochloride in the Synthesis of Heterocyclic Compounds
Rakitin O.A., Konstantinova L.S.
Advances in Heterocyclic Chemistry, 2008
3.
Heterocyclic Chemistry of Sulfur Chlorides – Fast Ways to Complex Heterocycles
García‐Valverde M., Torroba T.
European Journal of Organic Chemistry, 2006
7.
Konstantinova L.S., Rakitin O.A., Rees C.W., Amelichev S.A.
Mendeleev Communications, 2004
8.
Unprecedented conversion of triethylamine and disulfur dichloride into a thienopentathiepin and a heptathiocane
Konstantinova L.S., Rakitin O.A., Rees C.W., Souvorova L.I., Golovanov D.G., Lyssenko K.A.
Organic Letters, 2003
9.
A one-step synthesis of fused pentathiepins
Konstantinova L.S., Rakitin O.A., Rees C.W.
Chemical Communications, 2002
10.
Direct synthesis of fused 1,2,3,4,5-pentathiepins
Amelichev S.A., Konstantinova L.S., Lyssenko K.A., Rakitin O.A., Rees C.W.
Organic and Biomolecular Chemistry, 2005
11.
Amelichev S.A., Konstantinova L.S., Rakitin O.A., Rees C.W.
Mendeleev Communications, 2006
12.
10.1016/j.mencom.2009.03.001_bib9
Konstantinova
Izv. Akad. Nauk, Ser. Khim., 2006
13.
From Hünig's Base to Bis([1,2]dithiolo)- [1,4]thiazines in One Pot: The Fast Route to Highly Sulfurated Heterocycles
Rees C.W., Marcos C.F., Polo C., Torroba T., Rakitin O.A.
Angewandte Chemie International Edition in English, 1997
14.
Selective Syntheses of Bis[1,2]dithiolo[1,4]thiazines and Bis[1,2]dithiolopyrroles from Hünig's Base
Rees C.W., White A.J., Williams D.J., Rakitin O.A., Marcos C.F., Polo C., Torroba T.
Journal of Organic Chemistry, 1998
15.
Conversion of W-alkyldiisopropylàmines into yV,/V-bis(5-chloro-3-oxo[1,2]dithiol-4-yl)amines
Barriga S., Konstantinova L.S., Marcos C.F., Rakitin O.A., Rees C.W., Torroba T., White A.J., Williams D.J.
Journal of the Chemical Society Perkin Transactions 1, 1999
16.
Konstantinova L.S., Rakitin O.A., Rees C.W.
Mendeleev Communications, 2001
17.
Synthesis of bis[1,2]dithiolo[1,4]thiazine imines from Hünig’s base
Amelichev S.A., Barriga S., Konstantinova L.S., Markova T.B., Rakitin O.A., Rees C.W., Torroba T.
Journal of the Chemical Society Perkin Transactions 1, 2001
18.
Konstantinova L.S., Rakitin O.A., Rees C.W.
Mendeleev Communications, 2001
19.
Synthesis of bis[1,2]dithiolo[1,4]thiazines and a [1,2]dithiolo[1,4]thiazine from tertiary diisopropylamines
Rees C.W., White A.J., Williams D.J., Rakitin O.A., Konstantinova L.S., Marcos C.F., Torroba T.
Journal of Organic Chemistry, 1999
20.
A one-pot synthesis and 1,3-dipolar cycloaddition of [1,2]dithiolo[4,3-b]indole-3(4H)-thiones
Konstantinova L.S., Lysov K.A., Amelichev S.A., Obruchnikova N.V., Rakitin O.A.
Tetrahedron, 2009
21.
One-pot synthesis of 5-phenylimino, 5-thieno or 5-oxo-1,2,3-dithiazoles and evaluation of their antimicrobial and antitumor activity
Konstantinova L.S., Bol’shakov O.I., Obruchnikova N.V., Laborie H., Tanga A., Sopéna V., Lanneluc I., Picot L., Sablé S., Thiéry V., Rakitin O.A.
Bioorganic and Medicinal Chemistry Letters, 2009
22.
One pot synthesis of 1,2,3,-benzodithiazol-6-ones
Polo C., Ramos V., Torroba T., Rakitin O.A., Rees C.W.
Tetrahedron, 1998
23.
One-pot synthesis of indeno-l, 2-thiazines, -[l, 2]dithioles and thiophenes; new liquid crystalline materials
Konstantinova L.S., Rakitin O.A., Rees C.W., Souvorova L.I., Torroba T.
Journal of the Chemical Society Perkin Transactions 1, 1999
25.
Cyclopenta-1,2-dithioles, Cyclopenta-1,2-thiazines, and Methylenoindenes from New Molecular Rearrangements
Rakitin O.A., Rees C.W., Williams D.J., Torroba T.
Journal of Organic Chemistry, 1996
26.
Selective synthesis of bis[1,2]dithiolo[1,4]thiazines from 4-isopropylamino-5-chloro-1,2-dithiole-3-ones
Konstantinova L.S., Berezin A.A., Lysov K.A., Rakitin O.A.
Tetrahedron Letters, 2007
28.
One-pot synthesis of new liquid crystalline indeno heterocyclic materials
Konstantinova L.S., Rakitin O.A., Souvorova L.I., Rees C.W., White A.J., Williams D.J., Torroba T.
Chemical Communications, 1999
29.
Synthesis of 5H-1,2,3-Dithiazole, a Novel Heterocycle
Inamoto N., Okazaki R., Inoue K.
Heterocycles, 1981
30.
A novel oxime to pentathiepin cascade reaction
Macho S., Rodríguez T., Torroba T., Rees C.W.
Chemical Communications, 2001
31.
Y. Qi and Q. Wang, Chinese Patent, 2005, 1583741.
32.
Condensed Thiophenes and Selenophenes:  Thionyl Chloride and Selenium Oxychloride as Sulfur and Selenium Transfer Reagents
Amaresh R.R., Lakshmikantham M.V., Baldwin J.W., Cava M.P., Metzger R.M., Rogers R.D.
Journal of Organic Chemistry, 2002
33.
General synthetic system for 1,2,5-thiadiazoles
Weinstock L.M., Davis P., Handelsman B., Tull R.J.
Journal of Organic Chemistry, 1967
34.
1-(1,2,5-Thiadiazol-4-yl)-4-azatricyclo[2.2.1.02,6]heptanes as New Potent Muscarinic M1 Agonists:  Structure−Activity Relationship for 3-Aryl-2-propyn-1-yloxy and 3-Aryl-2-propyn-1-ylthio Derivatives
Jeppesen L., Olesen P.H., Hansen L., Sheardown M.J., Thomsen C., Rasmussen T., Jensen A.F., Christensen M.S., Rimvall K., Ward J.S., Whitesitt C., Calligaro D.O., Bymaster F.P., Delapp N.W., Felder C.C., et. al.
Journal of Medicinal Chemistry, 1999
35.
Resonance stabilized bis-thiadiazinyl radicals
Beer L., Haddon R.C., Itkis M.E., Leitch A.A., Oakley R.T., Reed R.W., Richardson J.F., VanderVeer D.G.
Chemical Communications, 2005