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Acid-catalyzed Rearrangement of O-Menthyl Methylthiocarbamate
| Content Provider | Scilit |
|---|---|
| Author | Kinoshita, Yoshiro Misaka, Michinori Kubota, Shuhei Ishikawa, Hisao |
| Copyright Year | 1977 |
| Description | Journal: Bioscience, Biotechnology, and Biochemistry O-Menthyl methylthiocarbamate was treated with boron trifluoride etherate producing S-menthyl methylthiocarbamate (4%) and S-p-menthan-8-yl methylthiocarbamate (56%). On the basis of this result, it was concluded that the rearrangement of secondary O-alkyl thiocarbamates proceeds by $S_{N}$1 mechanism whereas primary O-alkyl thiocarbamates rearrange by $S_{N}$2. |
| Related Links | https://www.tandfonline.com/doi/pdf/10.1080/00021369.1977.10862865?needAccess=true |
| Ending Page | 2360 |
| Page Count | 4 |
| Starting Page | 2357 |
| ISSN | 09168451 |
| e-ISSN | 13476947 |
| DOI | 10.1080/00021369.1977.10862865 |
| Journal | Bioscience, Biotechnology, and Biochemistry |
| Issue Number | 12 |
| Volume Number | 41 |
| Language | English |
| Publisher | Informa UK Limited |
| Publisher Date | 1977-12-01 |
| Access Restriction | Open |
| Subject Keyword | Journal: Bioscience, Biotechnology, and Biochemistry Organic Chemistry Boron Trifluoride Sn1 Mechanism Acid Catalyzed Alkyl Thiocarbamates Methylthiocarbamate Thiocarbamates Proceeds |
| Content Type | Text |
| Subject | Organic Chemistry Medicine Analytical Chemistry Molecular Biology Biochemistry Applied Microbiology and Biotechnology Biotechnology |