silyl esters

silyl esters
Макаров: силиловые эфиры, силиловые эфиры сложные

Универсальный англо-русский словарь. . 2011.

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  • Protecting group — A protecting group or protective group is introduced into a molecule by chemical modification of a functional group in order to obtain chemoselectivity in a subsequent chemical reaction. It plays an important role in multistep organic synthesis.… …   Wikipedia

  • Hexamethyldisiloxane — Chembox new Name = Hexamethyldisiloxane ImageFile = Hmds.png ImageName = IUPACName = Hexamethyldisiloxane OtherNames = HMDS HMDSO Bis(trimethylsilyl) ether Bis(trimethylsilyl) oxide Section1 = Chembox Identifiers SMILES = CSi(C)(C)OSi(C)(C)C… …   Wikipedia

  • Aldol reaction — The aldol reaction is a powerful means of forming carbon–carbon bonds in organic chemistry.[1][2][3] Discovered independently by …   Wikipedia

  • Polyester — For the 1981 motion picture, see Polyester (film). SEM picture of a bend in a high surface area polyester fiber with a seven lobed cross section …   Wikipedia

  • Trimethylsilyl chloride — Trimethylsilyl chloride …   Wikipedia

  • Lovastatin — Systematic (IUPAC) name (1S,3R,7S,8S …   Wikipedia

  • Organomanganese chemistry — is the chemistry of organometallic compounds containing a carbon to manganese chemical bond. In a recent review Cahiez et al. argue that as manganese is cheap and benign (only iron performs better in these aspects), organomanganese compounds have …   Wikipedia

  • Derivatization — Derivate redirects here. For various senses of its synonym derivative , see Derivative (disambiguation). Derivatization is a technique used in chemistry which transforms a chemical compound into a product (the reaction s derivate) of similar… …   Wikipedia

  • Sodium bis(trimethylsilyl)amide — Sodium bis(trimethylsilyl)amide …   Wikipedia

  • Acyloin — The structure of a typical acyloin. Acyloins (also referred to as ketols) are a class of organic compounds in organic chemistry sharing a common functional group consisting of a hydroxyl group placed on the α position of a carbonyl group.… …   Wikipedia

  • Desulfonylation reactions — are chemical reactions leading to the removal of a sulfonyl group from organic compounds. As the sulfonyl functional group is electron withdrawing, methods for cleaving the sulfur carbon bonds of sulfones are typically reductive in nature.… …   Wikipedia


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