Hydroxyl-directed stereoselective diboration of alkenes.
about
An in situ directing group strategy for chiral anion phase-transfer fluorination of allylic alcoholsEnantio- and Diastereoselective 1,2-Additions to α-Ketoesters with Diborylmethane and Substituted 1,1-Diborylalkanes.Transition-metal-free B-B and B-interelement reactions with organic molecules.Transition metal catalysis-a unique road map in the stereoselective synthesis of 1,3-polyols.Transition-Metal-Free Borylation of Allylic and Propargylic Alcohols.Copper-catalyzed cross-coupling reactions of epoxides with gem-diborylmethane: access to γ-hydroxyl boronic esters.Nickel-catalyzed synthesis of 1,1-diborylalkanes from terminal alkenes.Mechanism of NHC-Catalyzed Conjugate Additions of Diboron and Borosilane Reagents to α,β-Unsaturated Carbonyl Compounds.Regio- and Stereoselective Homologation of 1,2-Bis(Boronic Esters): Stereocontrolled Synthesis of 1,3-Diols and Sch 725674Carbohydrate-Catalyzed Enantioselective Alkene Diboration: Enhanced Reactivity of 1,2-Bonded Diboron Complexes.Selective uni- and bidirectional homologation of diborylmethane.Hydroxyl-Directed Cross-Coupling: A Scalable Synthesis of Debromohamigeran E and Other Targets of Interest.Substrate-Assisted, Transition-Metal-Free Diboration of Alkynamides with Mixed Diboron: Regio- and Stereoselective Access to trans-1,2-Vinyldiboronates.Undeniable Confirmation of the syn-Addition Mechanism for Metal-Free Diboration by Using the Crystalline Sponge Method.Amine Catalysis for the Organocatalytic Diboration of Challenging Alkenes.Homolytic Cleavage of a B-B Bond by the Cooperative Catalysis of Two Lewis Bases: Computational Design and Experimental Verification.Synergy of synthesis, computation and NMR reveals correct baulamycin structures.Reactivity of highly Lewis acidic diborane(4) towards pyridine and isocyanide: formation of boraalkene-pyridine complex and ortho-functionalized pyridine derivatives.Super electron donors derived from diboron.Enantio- and Diastereoselective Synthesis of Hydroxy Bis(boronates) via Cu-Catalyzed Tandem Borylation/1,2-Addition.Practical, efficient, and broadly applicable synthesis of readily differentiable vicinal diboronate compounds by catalytic three-component reactions.Substrate-Assisted, Transition-Metal-Free Diboration of Alkynamides with Mixed Diboron: Regio- and Stereoselective Access to trans -1,2-Vinyldiboronates
P2860
Q34282632-88C52E94-968E-453D-90AD-F6761C6F4AE6Q37209399-30440A83-89F1-426C-9B01-7E70868A2C99Q38784170-4BAAC672-3B47-4049-813D-5BC7A8E3831AQ39038143-F0EEE6FA-0A51-4704-8481-AB2118047174Q39397785-31ADA446-F8FC-472E-897C-37C6E698CB0FQ40359517-09F4BBD6-1F51-4319-87CC-4C072CF2530BQ40499084-0C74DDF8-5692-4656-9331-12BFED356E75Q41319490-98A3A295-720B-4AC5-9CD9-6F0B9C26091DQ41772288-7C90E42F-7B70-4210-AC28-F779E9B785B2Q42142551-2D97B6CB-B7E9-4112-B391-A3C0502E7EBFQ42293064-00F2BE10-E551-41D2-87E8-FADD6F74DC7CQ42738491-E1862733-1BC9-437D-BA56-198DFB661464Q45056249-802EBBC3-1728-4F01-92B7-61B73B581D4FQ48248000-E21C5B6B-F6D6-41E9-AD55-3DAF3DA43379Q48276386-E3E3FD32-2E37-4BA7-A90C-0FEB8B513F44Q50862858-F1CBBD2B-C580-4E3D-9A04-5D13FF713139Q51562219-3B5D95DB-80D9-4FD1-9AB5-177CC4CDB8F6Q52314841-EB7FE16D-4AE0-499C-B7FC-B29E89686594Q55056901-1BB6B4FC-A013-4DC6-9D6F-C9B66F0F2FAFQ55396228-7FAD182B-E413-4376-AB4D-3DC30797B126Q55396981-E8AB4B7C-E084-40E0-A17B-EBEF407A4335Q57449373-29C81E05-D87E-4080-B52E-F473C54C3EF6
P2860
Hydroxyl-directed stereoselective diboration of alkenes.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Hydroxyl-directed stereoselective diboration of alkenes.
@en
type
label
Hydroxyl-directed stereoselective diboration of alkenes.
@en
prefLabel
Hydroxyl-directed stereoselective diboration of alkenes.
@en
P2093
P2860
P356
P1476
Hydroxyl-directed stereoselective diboration of alkenes
@en
P2093
James P Morken
Liang Zhang
Thomas C Caya
Thomas P Blaisdell
P2860
P304
P356
10.1021/JA504228P
P407
P577
2014-06-24T00:00:00Z