A-new synthesis of N-sulfinylamines via β-elimination of chloroform from trichloromethanesulfinamides

Samuel Braverman; Marina Cherkinsky

doi:10.1016/s0040-4039(96)02351-9

A-new synthesis of N-sulfinylamines via β-elimination of chloroform from trichloromethanesulfinamides

Samuel Braverman
, Marina Cherkinsky

Department of Chemistry

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

9 Scopus citations

Abstract

The synthesis of various N-monosubstituted trichloromethanesulfinamides by two alternative and novel procedures is described. All these compounds have been found to undergo base-induced elimination of chloroform with formation of the corresponding N-sulfinylamines. Reaction proceeds smoothly under mild conditions.

Original language	English
Pages (from-to)	487-490
Number of pages	4
Journal	Tetrahedron Letters
Volume	38
Issue number	3
DOIs	https://doi.org/10.1016/s0040-4039(96)02351-9
State	Published - 20 Jan 1997

Bibliographical note

Funding Information:
This work was supported by the French Research National Agency (ANR) through the Vulnerability Milieu and Climate program (VULSACO project, No. ANR-06-VMC-009 ) and RELIEF MICROLIT . The authors benefitted from highly constructive discussions with D. Idier, (BRGM, Orléans, France). We thank a lot ATT technical and scientific translation company for the English corrections.

Funding

This work was supported by the French Research National Agency (ANR) through the Vulnerability Milieu and Climate program (VULSACO project, No. ANR-06-VMC-009 ) and RELIEF MICROLIT . The authors benefitted from highly constructive discussions with D. Idier, (BRGM, Orléans, France). We thank a lot ATT technical and scientific translation company for the English corrections.

Funders	Funder number
RELIEF MICROLIT
Agence Nationale de la Recherche	ANR-06-VMC-009

Access to Document

10.1016/s0040-4039(96)02351-9

Cite this

@article{4797e609cc824438ae62bdef6be53938,

title = "A-new synthesis of N-sulfinylamines via β-elimination of chloroform from trichloromethanesulfinamides",

abstract = "The synthesis of various N-monosubstituted trichloromethanesulfinamides by two alternative and novel procedures is described. All these compounds have been found to undergo base-induced elimination of chloroform with formation of the corresponding N-sulfinylamines. Reaction proceeds smoothly under mild conditions.",

author = "Samuel Braverman and Marina Cherkinsky",

note = "Funding Information: This work was supported by the French Research National Agency (ANR) through the Vulnerability Milieu and Climate program (VULSACO project, No. ANR-06-VMC-009 ) and RELIEF MICROLIT . The authors benefitted from highly constructive discussions with D. Idier, (BRGM, Orl{\'e}ans, France). We thank a lot ATT technical and scientific translation company for the English corrections.",

year = "1997",

month = jan,

day = "20",

doi = "10.1016/s0040-4039(96)02351-9",

language = "אנגלית",

volume = "38",

pages = "487--490",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Ltd.",

number = "3",

}

TY - JOUR

T1 - A-new synthesis of N-sulfinylamines via β-elimination of chloroform from trichloromethanesulfinamides

AU - Braverman, Samuel

AU - Cherkinsky, Marina

N1 - Funding Information: This work was supported by the French Research National Agency (ANR) through the Vulnerability Milieu and Climate program (VULSACO project, No. ANR-06-VMC-009 ) and RELIEF MICROLIT . The authors benefitted from highly constructive discussions with D. Idier, (BRGM, Orléans, France). We thank a lot ATT technical and scientific translation company for the English corrections.

PY - 1997/1/20

Y1 - 1997/1/20

N2 - The synthesis of various N-monosubstituted trichloromethanesulfinamides by two alternative and novel procedures is described. All these compounds have been found to undergo base-induced elimination of chloroform with formation of the corresponding N-sulfinylamines. Reaction proceeds smoothly under mild conditions.

AB - The synthesis of various N-monosubstituted trichloromethanesulfinamides by two alternative and novel procedures is described. All these compounds have been found to undergo base-induced elimination of chloroform with formation of the corresponding N-sulfinylamines. Reaction proceeds smoothly under mild conditions.

UR - https://www.scopus.com/pages/publications/0031021710

U2 - 10.1016/s0040-4039(96)02351-9

DO - 10.1016/s0040-4039(96)02351-9

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???

AN - SCOPUS:0031021710

SN - 0040-4039

VL - 38

SP - 487

EP - 490

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 3

ER -

A-new synthesis of N-sulfinylamines via β-elimination of chloroform from trichloromethanesulfinamides

Abstract

Bibliographical note

Funding

Access to Document

Other files and links

Fingerprint

Cite this