Asymmetric catalytic N-phosphonyl imine chemistry: the use of primary free amino acids and Et2AlCN for asymmetric catalytic Strecker reaction.
about
REGIOSELECTIVE MULTICOMPONENT DOMINO REACTIONS PROVIDING RAPID AND EFFICIENT ROUTES TO FUSED ACRIDINESAsymmetric synthesis of α-amino-1,3-dithianes via chiral N-phosphonyl imine-based Umpolung reaction without using chromatography and recrystallization.Microwave-assisted multicomponent reaction in water leading to highly regioselective formation of benzo[f]azulen-1-ones.Approach to vicinal t-Boc-amino dibromides via catalytic aminobromination of nitrostyrenes without using chromatography and recrystallization.N-Phosphonyl/phosphinyl imines and group-assisted purification (GAP) chemistry/technology.Design, synthesis, and applications of chiral N-2-phenyl-2-propyl sulfinyl imines for group-assisted purification (GAP) asymmetric synthesisSolution-phase-peptide synthesis via the group-assisted purification (GAP) chemistry without using chromatography and recrystallization.Efficient domino approaches to multifunctionalized fused pyrroles and dibenzo[b,e][1,4]diazepin-1-ones.A highly efficient group-assisted purification method for the synthesis of poly-functionalized pyrimidin-5-yl-pyrroles via one-pot four-component domino reaction.A highly enantioselective catalytic Strecker reaction of cyclic (Z)-aldimines.Asymmetric aza-Morita-Baylis-Hillman reactions of chiral N-phosphonyl imines with acrylates via GAP chemistry/technology.An efficient three-component synthesis of highly functionalized tetrahydroacenaphtho[1,2-b]indolone derivatives catalyzed by L-proline.Clean and efficient synthesis of isoxazole derivatives in aqueous media.
P2860
Q34429069-CB6FB368-3D8E-4EA2-A112-B12AE3FCB1A9Q34778869-468688FA-A519-4096-9097-9594796439F5Q35072405-236A3542-4CDB-4287-ABFD-97057FC956D2Q36600200-1FD25F12-EF5D-4772-862B-3BE9599D85F8Q38293533-3C7C8EFD-4A1E-4977-B0D4-7B1D72705E25Q39972709-12EA0D1D-08FC-43EB-B9D2-04947386B82BQ41965730-A5FC5855-8335-43C0-AA69-01B279BEA6C6Q42145721-F9693DB2-1A0A-47F4-92AC-A044E13BECF0Q50450304-2B7A5605-4473-460B-989A-BAD2E4534B95Q50499122-D936CF42-C199-47FA-9EF8-1F59F5B2F244Q51315056-6D3C3DE7-FB88-4DDA-A657-7E1230E5C946Q53466556-BEDB4FDB-08B8-4E91-9567-85ED9BF04643Q53676553-EA8CA70B-9611-4AD5-8AC6-4DAC5FC7777D
P2860
Asymmetric catalytic N-phosphonyl imine chemistry: the use of primary free amino acids and Et2AlCN for asymmetric catalytic Strecker reaction.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Asymmetric catalytic N-phospho ...... c catalytic Strecker reaction.
@en
Asymmetric catalytic N-phospho ...... c catalytic Strecker reaction.
@nl
type
label
Asymmetric catalytic N-phospho ...... c catalytic Strecker reaction.
@en
Asymmetric catalytic N-phospho ...... c catalytic Strecker reaction.
@nl
prefLabel
Asymmetric catalytic N-phospho ...... c catalytic Strecker reaction.
@en
Asymmetric catalytic N-phospho ...... c catalytic Strecker reaction.
@nl
P2093
P2860
P356
P1476
Asymmetric catalytic N-phospho ...... c catalytic Strecker reaction.
@en
P2093
Parminder Kaur
Suresh Pindi
Trideep Rajale
Walter Wever
P2860
P304
P356
10.1021/JO100865Q
P407
P577
2010-08-01T00:00:00Z