Cargando…
A selective synthesis of 4-aminobiphenyl-N2-deoxyguanosine adducts.
A selective synthesis of N2-deoxyguanosine adducts derived from 4-aminobiphenyl (ABP) is described. The reactions of O2-trifluoromethylsulfonyl-O6-allyl-3',5'-O-bis(tert-butyldimethyl silyl)-2'- deoxyxanthosine with 3-amino-4-acetaminobiphenyl and 4-hydrazinobiphenyl, respectively, ar...
Autores principales: | , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
1994
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566842/ https://www.ncbi.nlm.nih.gov/pubmed/7889838 |
_version_ | 1782129703905132544 |
---|---|
author | Scheer, S Steinbrecher, T Boche, G |
author_facet | Scheer, S Steinbrecher, T Boche, G |
author_sort | Scheer, S |
collection | PubMed |
description | A selective synthesis of N2-deoxyguanosine adducts derived from 4-aminobiphenyl (ABP) is described. The reactions of O2-trifluoromethylsulfonyl-O6-allyl-3',5'-O-bis(tert-butyldimethyl silyl)-2'- deoxyxanthosine with 3-amino-4-acetaminobiphenyl and 4-hydrazinobiphenyl, respectively, are the key steps. Successive removal of the protecting groups from the protected adducts leads to the free adducts 3-(deoxyguanosine-N2-yl)-acetyl-ABP and N-(deoxyguanosyl-N2-yl)-ABP, respectively. |
format | Text |
id | pubmed-1566842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1994 |
record_format | MEDLINE/PubMed |
spelling | pubmed-15668422006-09-19 A selective synthesis of 4-aminobiphenyl-N2-deoxyguanosine adducts. Scheer, S Steinbrecher, T Boche, G Environ Health Perspect Research Article A selective synthesis of N2-deoxyguanosine adducts derived from 4-aminobiphenyl (ABP) is described. The reactions of O2-trifluoromethylsulfonyl-O6-allyl-3',5'-O-bis(tert-butyldimethyl silyl)-2'- deoxyxanthosine with 3-amino-4-acetaminobiphenyl and 4-hydrazinobiphenyl, respectively, are the key steps. Successive removal of the protecting groups from the protected adducts leads to the free adducts 3-(deoxyguanosine-N2-yl)-acetyl-ABP and N-(deoxyguanosyl-N2-yl)-ABP, respectively. 1994-10 /pmc/articles/PMC1566842/ /pubmed/7889838 Text en |
spellingShingle | Research Article Scheer, S Steinbrecher, T Boche, G A selective synthesis of 4-aminobiphenyl-N2-deoxyguanosine adducts. |
title | A selective synthesis of 4-aminobiphenyl-N2-deoxyguanosine adducts. |
title_full | A selective synthesis of 4-aminobiphenyl-N2-deoxyguanosine adducts. |
title_fullStr | A selective synthesis of 4-aminobiphenyl-N2-deoxyguanosine adducts. |
title_full_unstemmed | A selective synthesis of 4-aminobiphenyl-N2-deoxyguanosine adducts. |
title_short | A selective synthesis of 4-aminobiphenyl-N2-deoxyguanosine adducts. |
title_sort | selective synthesis of 4-aminobiphenyl-n2-deoxyguanosine adducts. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1566842/ https://www.ncbi.nlm.nih.gov/pubmed/7889838 |
work_keys_str_mv | AT scheers aselectivesynthesisof4aminobiphenyln2deoxyguanosineadducts AT steinbrechert aselectivesynthesisof4aminobiphenyln2deoxyguanosineadducts AT bocheg aselectivesynthesisof4aminobiphenyln2deoxyguanosineadducts AT scheers selectivesynthesisof4aminobiphenyln2deoxyguanosineadducts AT steinbrechert selectivesynthesisof4aminobiphenyln2deoxyguanosineadducts AT bocheg selectivesynthesisof4aminobiphenyln2deoxyguanosineadducts |