Highly Enantioselective Catalytic Alkynylation of Ketones – A Convenient Approach to Optically Active Propargylic Alcohols

Gui Lu; Xingshu Li; Yue-Ming Li; Fuk Yee Kwong; Albert S. C. Chan

doi:10.1002/adsc.200606078

Highly Enantioselective Catalytic Alkynylation of Ketones – A Convenient Approach to Optically Active Propargylic Alcohols

Advanced Synthesis & Catalysis ◽

10.1002/adsc.200606078 ◽

2006 ◽

Vol 348 (14) ◽

pp. 1926-1933 ◽

Cited By ~ 54

Author(s):

Gui Lu ◽

Xingshu Li ◽

Yue-Ming Li ◽

Fuk Yee Kwong ◽

Albert S. C. Chan

Keyword(s):

Optically Active ◽

Propargylic Alcohols ◽

Convenient Approach

Download Full-text

Highly Enantioselective Catalytic Alkynylation of Ketones — A Convenient Approach to Optically Active Propargylic Alcohols.

ChemInform ◽

10.1002/chin.200704072 ◽

2007 ◽

Vol 38 (4) ◽

Author(s):

Gui Lu ◽

Xingshu Li ◽

Yue-Ming Li ◽

Fuk Yee Kwong ◽

Albert S. C. Chan

Keyword(s):

Optically Active ◽

Propargylic Alcohols ◽

Convenient Approach

Download Full-text

ChemInform Abstract: Catalytic, Enantioselective Acetate Aldol Additions to α,β-Ynals: Preparation of Optically Active Propargylic Alcohols.

ChemInform ◽

10.1002/chin.199840085 ◽

2010 ◽

Vol 29 (40) ◽

pp. no-no

Author(s):

R. A. SINGER ◽

M. S. SHEPARD ◽

E. M. CARREIRA

Keyword(s):

Optically Active ◽

Propargylic Alcohols ◽

Aldol Additions

Download Full-text

CaF2 catalyzed SN2 type chlorodehydroxylation of chiral secondary alcohols with thionyl chloride: a practical and convenient approach for the preparation of optically active chloroalkanes

Tetrahedron Letters ◽

10.1016/j.tetlet.2013.02.079 ◽

2013 ◽

Vol 54 (18) ◽

pp. 2261-2263 ◽

Cited By ~ 6

Author(s):

Junjie Zhang ◽

Huanxia Wang ◽

Yun Ma ◽

Youming Wang ◽

Zhenghong Zhou ◽

...

Keyword(s):

Thionyl Chloride ◽

Optically Active ◽

Secondary Alcohols ◽

Convenient Approach

Download Full-text

Enzymatic desymmetrization of 3-alkyl- and 3-arylglutaronitriles, a simple and convenient approach to optically active 4-amino-3-phenylbutanoic acids

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(02)00028-9 ◽

2002 ◽

Vol 12 (24) ◽

pp. 3367-3373 ◽

Cited By ~ 37

Author(s):

Mei-Xiang Wang ◽

Chu-Sheng Liu ◽

Ji-Sheng Li

Keyword(s):

Optically Active ◽

Convenient Approach ◽

Enzymatic Desymmetrization

Download Full-text

Efficient Synthesis of Optically Active 2,3-Allenols via the Simple CuBr-Mediated Reaction of Optically Active Propargylic Alcohols with Paraformaldehyde.

ChemInform ◽

10.1002/chin.200302061 ◽

2003 ◽

Vol 34 (2) ◽

Author(s):

Shengming Ma ◽

Hairong Hou ◽

Shimin Zhao ◽

Guangwei Wang

Keyword(s):

Optically Active ◽

Efficient Synthesis ◽

Propargylic Alcohols

Download Full-text

Novozym-435-catalyzed enzymatic separation of racemic propargylic alcohols. A facile route to optically active terminal aryl propargylic alcohols

Tetrahedron Letters ◽

10.1016/s0040-4039(03)01528-4 ◽

2003 ◽

Vol 44 (33) ◽

pp. 6343-6346 ◽

Cited By ~ 48

Author(s):

Daiwang Xu ◽

Zuyi Li ◽

Shengming Ma

Keyword(s):

Optically Active ◽

Novozym 435 ◽

Propargylic Alcohols ◽

Facile Route

Download Full-text

ChemInform Abstract: Thiophosphoramide-Catalyzed Asymmetric Michael Addition of Acetone to Functionalized Nitrostyrenes: A Convenient Approach to Optically Active Tetrahydropyrans.

ChemInform ◽

10.1002/chin.201122139 ◽

2011 ◽

Vol 42 (22) ◽

pp. no-no

Author(s):

Yang Wu ◽

Aidang Lu ◽

Yunfeng Liu ◽

Xiaolei Yu ◽

Youming Wang ◽

...

Keyword(s):

Michael Addition ◽

Optically Active ◽

Asymmetric Michael Addition ◽

Convenient Approach

Download Full-text

Thiophosphoramide catalyzed asymmetric Michael addition of acetone to functionalized nitrostyrenes: a convenient approach to optically active tetrahydropyrans

Tetrahedron Asymmetry ◽

10.1016/j.tetasy.2010.11.019 ◽

2010 ◽

Vol 21 (24) ◽

pp. 2988-2992 ◽

Cited By ~ 23

Author(s):

Yang Wu ◽

Aidang Lu ◽

Yunfeng Liu ◽

Xiaolei Yu ◽

Youming Wang ◽

...

Keyword(s):

Michael Addition ◽

Optically Active ◽

Asymmetric Michael Addition ◽

Convenient Approach

Download Full-text

ChemInform Abstract: CaF2-Catalyzed SN2-type Chlorodehydroxylation of Chiral Secondary Alcohols with Thionyl Chloride: A Practical and Convenient Approach for the Preparation of Optically Active Chloroalkanes.

ChemInform ◽

10.1002/chin.201332043 ◽

2013 ◽

Vol 44 (32) ◽

pp. no-no

Author(s):

Junjie Zhang ◽

Huanxia Wang ◽

Yun Ma ◽

Youming Wang ◽

Zhenghong Zhou ◽

...

Keyword(s):

Thionyl Chloride ◽

Optically Active ◽

Secondary Alcohols ◽

Convenient Approach

Download Full-text

Palladium/H+-cocatalyzed kinetic resolution of tertiary propargylic alcohols

Chemical Communications ◽

10.1039/c8cc01949e ◽

2018 ◽

Vol 54 (47) ◽

pp. 6064-6067 ◽

Cited By ~ 16

Author(s):

Wanli Zhang ◽

Shengming Ma

Keyword(s):

Kinetic Resolution ◽

Optically Active ◽

Propargylic Alcohols

A new concept for the synthesis of optically active tertiary propargylic alcohols with 90–99% ee through palladium/H+-cocatalyzed kinetic resolution was developed.

Download Full-text