Molecular Iodine-Catalyzed Highly Stereoselective Synthesis of Sugar Acetylenes.

ChemInform ◽  
2003 ◽  
Vol 34 (20) ◽  
Author(s):  
J. S. Yadav ◽  
B. V. S. Reddy ◽  
C. V. Rao ◽  
M. Sridhar Reddy
Keyword(s):  
Stereoselective Synthesis ◽  
Molecular Iodine

Molecular Iodine-Catalyzed Highly Stereoselective Synthesis of Sugar Acetylenes­

Synthesis ◽  
2003 ◽  
pp. 0247-0250 ◽  
Author(s):  
J. S. Yadav ◽  
B. V. Reddy ◽  
C. V. Rao ◽  
M. Sridhar Reddy
Keyword(s):  
Stereoselective Synthesis ◽  
Molecular Iodine

Iodine promoted iodosulfonylation of alkynes with sulfonyl hydrazides in an aqueous medium: highly stereoselective synthesis of (E)-β-iodo vinylsulfones

2018 ◽  
Vol 42 (11) ◽  
pp. 8752-8755 ◽  
Author(s):  
Yunlei Hou ◽  
Liangyu Zhu ◽  
Hao Hu ◽  
Shaowei Chen ◽  
Zefei Li ◽  
...  
Keyword(s):  
Aqueous Medium ◽  
Stereoselective Synthesis ◽  
Molecular Iodine

An efficient, molecular iodine-promoted MCR of alkynes and sulfonyl hydrazide for the synthesis of (E)-β-iodo vinylsulfone derivatives has been developed.

Highly Stereoselective Synthesis of 2,3-Unsaturated Thioglycopyranosides Employing Molecular Iodine

Synthesis ◽  
2010 ◽  
Vol 2010 (10) ◽  
pp. 1617-1620 ◽  
Author(s):  
Basi Reddy ◽  
Ch. Divyavani ◽  
Jhillu Yadav
Keyword(s):  
Stereoselective Synthesis ◽  
Molecular Iodine

ChemInform Abstract: Highly Stereoselective Synthesis of 2,3-Unsaturated Thioglycopyranosides Employing Molecular Iodine.

ChemInform ◽  
2010 ◽  
Vol 41 (39) ◽  
pp. no-no
Author(s):  
Basi V. Subba Reddy ◽  
Ch. Divyavani ◽  
Jhillu S. Yadav
Keyword(s):  
Stereoselective Synthesis ◽  
Molecular Iodine

An iodine catalyzed metal free domino process for the stereoselective synthesis of oxygen bridged bicyclic ethers

2015 ◽  
Vol 13 (24) ◽  
pp. 6737-6741 ◽  
Author(s):  
B. V. Subba Reddy ◽  
B. Someswarao ◽  
N. Prudhviraju ◽  
B. Jagan Mohan Reddy ◽  
B. Sridhar ◽  
...  
Keyword(s):  
Stereoselective Synthesis ◽  
High Selectivity ◽  
Molecular Iodine ◽  
Metal Free

A domino cyclization of 4-(2-hydroxyethyl)cyclohex-3-enol with aldehydes using 10 mol% molecular iodine is reported to produce oxygen bridged bicyclic ethers in good yields with high selectivity.

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