September 23, 2024, 04:24:03 PM
Forum Rules: Read This Before Posting


Topic: Mannose triflate  (Read 1732 times)

0 Members and 1 Guest are viewing this topic.

Offline Sami.allmed

  • Very New Member
  • *
  • Posts: 2
  • Mole Snacks: +0/-0
Mannose triflate
« on: October 19, 2015, 11:50:37 PM »
Hi , i am working as medical system engineer and working on cyclotron project, while reading its chemical process one confusion occur related to mannose triflate which i am unable to solve uptill now, so please help me,

i want to know why mannose triflate is written as

 1,3,4,6–O–Acetyl–2–O–trifluoro-methanesulfonyl–beta–D–mannopyranose (mannose triflate).

and why 1,3,4,5–O–Acetyl–2–O–trifluoro-methanesulfonyl–beta–D–mannopyranose (mannose triflate) is not correct

because acetyl group is on 5th carbon not on sixth and also there is something unsual on sixth carbon i.e oxygen inplace of carbon,

Kindly help me in understanding this formula.

link for mannose triflate formula is here

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3097819/figure/F7/

Thanks

Offline mjc123

  • Chemist
  • Sr. Member
  • *
  • Posts: 2069
  • Mole Snacks: +302/-12
Re: Mannose triflate
« Reply #1 on: October 20, 2015, 04:39:51 AM »
Look more carefully. The substituent on C5 is not OAc, it is CH2OAc. Hence the OAc is on C6.

Offline Sami.allmed

  • Very New Member
  • *
  • Posts: 2
  • Mole Snacks: +0/-0
Re: Mannose triflate
« Reply #2 on: October 20, 2015, 06:28:08 AM »
Thank you so much :)

Sponsored Links