Web25 apr. 2024 · Chapter 2: Monomethoxytrityl (MMTr) as an Efficient S-Protecting Group in the Manipulation of Glycosyl Thiols by Raymond Smith, Xiangming Zhu, and Elena … WebDescribed herein are compounds and compositions characterized, in certain embodiments, by conjugation of various groups, such as lipophilic groups, to an amino or amide group of a
MMTr as an efficient anomeric S-protecting group for the …
WebIf you want to protect an NH group for heterocycles such as indole, then the best protection group is the phenylsulfonyl (PhSO2) but while introduction is quite easy from the PhSO2Cl, the... WebPROTECTING GROUPS 60 Methoxytrityl Ethers JACS 1962, 84, 430 - methoxy group(s) make it easier to remove R 2 C O R R 1 R 3 (p-Methoxyphenyl)diphenylmethyl ether 4' … shutterfly amanda pyk
Chapter 2: Monomethoxytrityl (MMTr) as an Efficient S-Protecting …
WebYou probably don't need a protecting group. I've carried tBuOH through into a Swearn/Wittig sequence. I've even run a cuperate addition in the presence of a tertiary … WebPhosphate deprotection is the removal of the cyanoethyl protecting groups from the phosphate backbone. Base deprotection is the removal of the protecting groups on the bases or modifier. There are many considerations when approaching oligo deprotection, as shown in the Box on the right. WebMonomethoxytrityl (MMTr) as an Efficient S-Protecting Group in the Manipulation of Glycosyl Thiols book. By Raymond Smith, Xiangming Zhu, Elena Calatrava-Pérez. Book Carbohydrate Chemistry. Click here to navigate to parent product. Edition 1st Edition. First Published 2024. Imprint CRC Press. Pages 8. shutterfly and free shipping