Discrimination of remote chirality of primary alcohols using 1,1′-binaphthyl-2,2′-DIYL phosphoroselenoyl chlorides as a chiral molecular tool

2016 ◽  
Vol 191 (2) ◽  
pp. 163-173 ◽  
Author(s):  
Toshiaki Murai ◽  
Hikaru Itoh
Keyword(s):  
Primary Alcohols ◽  
Molecular Tool

Addition of primary alcohols to 3-chlorononafluoro-1,5-hexadiene and perfluoro-1,3,5-hexatriene

1985 ◽  
Vol 50 (8) ◽  
pp. 1714-1726 ◽  
Author(s):  
Václav Dědek ◽  
Igor Linhart ◽  
Milan Kováč
Keyword(s):  
Sulfuric Acid ◽  
Primary Alcohols ◽  
Principal Product ◽  
Allyl Rearrangement ◽  
Concentrated Sulfuric Acid ◽  
Sodium Alkoxide

Sodium alkoxide-catalyzed addition of methanol, ethanol and propanol to 3-chlorononafluoro-1,5-hexadiene (I) proceeds at temperatures -35 °C to 8 °C with allyl rearrangement, affording 1,6-dialkoxy-1,1,2,3,4,4,5,6,6-octafluoro-2,4-hexadiene (V) as the principal product, along with 1,6-dialkoxy-1,2,3,3,4,5,6,6-octafluoro-1,5-diene (VI) and trans-1,6-dialkoxy-1,1,2,3,4,4,5,6,6-nonafluoro-2-hexene (VII). The ethers Va-Vc consist of the cis,trans- and trans,trans-isomers in about 3 : 1 ratio, whereas the ethers VIa-VIc have trans,trans-configuration. Ethers Vc and VIc react with concentrated sulfuric acid to give dipropyl 2,3,4,5-tetrafluoro-2,4-hexadienedioate (IX) and dipropyl 2,3,4,4,5-pentafluoro-2-hexenedioate (X), respectively, whereas the ether VIIc affords a mixture of propyl 6-propyloxy-2,3,4,4,5,6-heptafluoro-2-hexenoate (XI) and ester X. Addition of methanol to perfluoro-1,3,5-hexatriene (II) affords 1,1,2,3,4,5,6,6-octafluoro-1,6-dimethoxy-3-hexene (XIII) as the principal product.

Cross β-alkylation of primary alcohols catalysed by DMF-stabilized iridium nanoparticles

2021 ◽  
Author(s):  
Masaki Kobayashi ◽  
Hiroki Yamaguchi ◽  
Takeyuki Suzuki ◽  
Yasushi Obora
Keyword(s):  
Primary Alcohols ◽  
Recycling Process ◽  
Catalyst Recycling ◽  
Simple Method ◽  
Benzyl Alcohols ◽  
Effective Catalyst ◽  
Iridium Nanoparticles ◽  
Highly Effective ◽  
Linear Alcohols ◽  
The Cross

A simple method for the cross β-alkylation of linear alcohols with benzyl alcohols in the presence of DMF-stabilized iridium nanoparticles was developed. Furthermore, a highly effective catalyst-recycling process was also developed.

BnA1.CER4 and BnC1.CER4 are redundantly involved in branched primary alcohols in the cuticle wax of Brassica napus

2021 ◽  
Author(s):  
Jie Liu ◽  
Lixia Zhu ◽  
Benqi Wang ◽  
Huadong Wang ◽  
Imran khan ◽  
...  
Keyword(s):  
Brassica Napus ◽  
Primary Alcohols

A novel, one-step method for the conversion of primary alcohols into carbamate-protected amines

2002 ◽  
Vol 43 (21) ◽  
pp. 3887-3890 ◽  
Author(s):  
Michael R. Wood ◽  
June Y. Kim ◽  
Kathy M. Books
Keyword(s):  
Primary Alcohols ◽  
Step Method ◽  
One Step

Nickel-catalysed dehydrogenative coupling of aromatic diamines with alcohols: selective synthesis of substituted benzimidazoles and quinoxalines

2019 ◽  
Vol 55 (42) ◽  
pp. 5958-5961 ◽  
Author(s):  
Atanu Bera ◽  
Motahar Sk ◽  
Khushboo Singh ◽  
Debasis Banerjee
Keyword(s):  
Hydrogen Gas ◽  
Selective Synthesis ◽  
Primary Alcohols ◽  
Aromatic Diamines ◽  
Dehydrogenative Coupling

The nickel-catalysed dehydrogenative coupling of 1,2-di-amino-benzene with primary alcohols and diols for the synthesis of N-heterocycles is reported. The catalytic protocol enables the transformation in up to 91% yield and generates water and hydrogen gas as byproducts.

Selective Acceptorless Conversion of Primary Alcohols to Acetals and Dihydrogen Catalyzed by the Ruthenium(II) Complex Ru(PPh3)2(NCCH3)2(SO4)

2012 ◽  
Vol 354 (2-3) ◽  
pp. 497-504 ◽  
Author(s):  
Elizaveta Kossoy ◽  
Yael Diskin-Posner ◽  
Gregory Leitus ◽  
David Milstein
Keyword(s):  
Primary Alcohols
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