Home / Articles / Reagents for the preparation and cleavage of 1,3-dithiolanes

Reagents for the preparation and cleavage of 1,3-dithiolanes

Ajoy K Banerjee 1
Ajoy K Banerjee
, 
M S Laya Mimo 1
M S Laya Mimo
1 H. E. J. Research Institute of Chemistry International Center for Chemical and Biological Sciences, Caracas
10.1070/RC2000v069n11ABEH000583
Published 30 November 1999
Communication , Volume 69, Issue 11, 947-955
32
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Banerjee A. K., Laya Mimo M. S. Reagents for the preparation and cleavage of 1,3-dithiolanes // Russian Chemical Reviews. 2000. Vol. 69. No. 11. pp. 947-955.
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Banerjee A. K., Laya Mimo M. S. Reagents for the preparation and cleavage of 1,3-dithiolanes // Russian Chemical Reviews. 2000. Vol. 69. No. 11. pp. 947-955.
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TY - JOUR
DO - 10.1070/RC2000v069n11ABEH000583
UR - https://rcr.colab.ws/publications/10.1070/RC2000v069n11ABEH000583
TI - Reagents for the preparation and cleavage of 1,3-dithiolanes
T2 - Russian Chemical Reviews
AU - Banerjee, Ajoy K
AU - Laya Mimo, M S
PY - 2000
DA - 1999/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 947-955
IS - 11
VL - 69
ER -
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@article{2000_Banerjee,
author = {Ajoy K Banerjee and M S Laya Mimo},
title = {Reagents for the preparation and cleavage of 1,3-dithiolanes},
journal = {Russian Chemical Reviews},
year = {2000},
volume = {69},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC2000v069n11ABEH000583},
number = {11},
pages = {947--955},
doi = {10.1070/RC2000v069n11ABEH000583}
}
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Banerjee, Ajoy K., and M S Laya Mimo. “Reagents for the preparation and cleavage of 1,3-dithiolanes.” Russian Chemical Reviews, vol. 69, no. 11, Nov. 2000, pp. 947-955. https://rcr.colab.ws/publications/10.1070/RC2000v069n11ABEH000583.
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Abstract

Data on procedures for protection of the carbonyl group by its conversion into the 1,3-dithiolane moiety and on cleavage of the latter under the action of different reagents are surveyed. The preparation of 1,3-dithiolanes from carbonyl compounds followed by deprotection can be used in syntheses of various organic compounds. The bibliography includes 54 references.

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