about
Synthesis of the 1-monoester of 2-ketoalkanedioic acids, for example, octyl α-ketoglutarateOzonolysis of the double bond of the unsaturated uronate residue in low-molecular-weight heparin and K5 heparosan.The transition from the open minimum to the ring minimum on the ground state and on the lowest excited state of like symmetry in ozone: A configuration interaction study.Synthesis of five- and six-membered cyclic organic peroxides: Key transformations into peroxide ring-retaining products.On-line analysis of a continuous-flow ozonolysis reaction using Raman spectroscopy.Liquid phase oxidation chemistry in continuous-flow microreactors.Criegee intermediate-hydrogen sulfide chemistry at the air/water interfacePyridine is an organocatalyst for the reductive ozonolysis of alkenes.Tandem application of C-C bond-forming reactions with reductive ozonolysis.D-Arabinose-based synthesis of homo-C-d4T and homo-C-thymidine.Gold-catalyzed carboalkoxylations of 2-ethynylbenzyl ethers to form 1- and 3-substituted 2-methoxy-1-H-indenes: Brønsted acids versus gold catalysis.Enzymatic aerobic alkene cleavage catalyzed by a Mn(3+) -dependent proteinase a homologue.New insights into 1,2,4-trioxolane stability and the crucial role of ozone in promoting polymer degradation.Substituent effects on the spectroscopic properties of Criegee intermediates.De novo chemoenzymatic synthesis of sialic acidEnd-group differentiating ozonolysis of furocoumarinsMetal or No Metal: That Is the Question!
P2860
Q33904269-32ED38A9-0DBE-4078-A9BB-2F7BB8F2C0DFQ33956418-B519AB81-45C9-48A1-91A8-C22EB935287CQ36678245-6EF1FEDA-9F3B-4F56-A0F4-25C21D95B976Q38181092-4BDB5248-66AE-4979-A6C1-40E4E933B9A1Q38503863-56BC4E1E-28D1-43DE-B047-913315790AD3Q38552619-9CFC0599-B11D-4295-93EF-6D341E7C5945Q41856737-4ECA4064-3F12-4DB1-ACB2-AD3CD45F7EA6Q42146959-1FF44328-A0B7-4A8F-B4F9-090F1C4589E3Q42534969-EAF62ADE-8A47-4E06-81F6-77F85B6B8FB2Q43150283-1324A526-BAD1-4DEB-8F5F-15F17EEF3532Q44027237-5817BE88-6BB6-4E92-8259-8416C18F0941Q44764703-C931A2A2-F546-414E-9422-E5EE50863598Q45779270-644768DC-2CBC-475C-8180-4B8523EB5CB1Q46269964-2730C77E-A26A-4031-A91D-952E03988D6AQ57563976-EA26D0D2-DE0F-4A13-85EE-77AC33B83C2AQ57833453-28DD163D-FCDC-46E5-9A5F-A10E12073475Q58214138-61A1FC75-C170-4C16-894D-3734072CB446
P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Ozonolysis applications in drug synthesis.
@ast
Ozonolysis applications in drug synthesis.
@en
type
label
Ozonolysis applications in drug synthesis.
@ast
Ozonolysis applications in drug synthesis.
@en
prefLabel
Ozonolysis applications in drug synthesis.
@ast
Ozonolysis applications in drug synthesis.
@en
P2093
P356
P1433
P1476
Ozonolysis applications in drug synthesis.
@en
P2093
Richard Pariza
Robin M Champeau
Scott G Van Ornum
P304
P356
10.1021/CR040682Z
P577
2006-07-01T00:00:00Z