ChemInform Abstract: TOTAL SYNTHESIS OF (-)-NEPLANOCIN A

1984 ◽  
Vol 15 (17) ◽  
Author(s):  
M.-I. LIM ◽  
V. E. MARQUEZ
Keyword(s):  
Total Synthesis ◽  
Neplanocin A

ChemInform Abstract: A Formal Total Synthesis of (.+-.)-Neplanocin A.

ChemInform ◽  
2008 ◽  
Vol 39 (1) ◽  
Author(s):  
Faiz Ahmed Khan ◽  
Bhimsen Rout
Keyword(s):  
Total Synthesis ◽  
Neplanocin A

Total Synthesis of (-)-Neplanocin A from L-Ribulose

Synlett ◽  
1991 ◽  
Vol 1991 (12) ◽  
pp. 921-922 ◽  
Author(s):  
K. Vanhessche ◽  
C. González Bello ◽  
M. Vandewalle
Keyword(s):  
Total Synthesis ◽  
Neplanocin A

A Formal Total Synthesis of (±)-Neplanocin A

2007 ◽  
Vol 72 (18) ◽  
pp. 7011-7013 ◽  
Author(s):  
Faiz Ahmed Khan ◽  
Bhimsen Rout
Keyword(s):  
Total Synthesis ◽  
Neplanocin A

Total synthesis of (-)-neplanocin A

1988 ◽  
Vol 53 (24) ◽  
pp. 5709-5714 ◽  
Author(s):  
Victor E. Marquez ◽  
Mu Ill Lim ◽  
Christopher K. H. Tseng ◽  
Anica Markovac ◽  
Matthew A. Priest ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Neplanocin A

ChemInform Abstract: Total Synthesis of (-)-Neplanocin A by Using Lithium Thiolate-Initiated Michael-Aldol Tandem Cyclization Reaction.

ChemInform ◽  
2010 ◽  
Vol 33 (21) ◽  
pp. no-no
Author(s):  
Masashi Ono ◽  
Katsumi Nishimura ◽  
Hiroshi Tsubouchi ◽  
Yasuo Nagaoka ◽  
Kiyoshi Tomioka
Keyword(s):  
Total Synthesis ◽  
Cyclization Reaction ◽  
Neplanocin A ◽  
Tandem Cyclization

Total Synthesis of (−)-Neplanocin A by Using Lithium Thiolate-Initiated Michael−Aldol Tandem Cyclization Reaction

2001 ◽  
Vol 66 (24) ◽  
pp. 8199-8203 ◽  
Author(s):  
Masashi Ono ◽  
Katsumi Nishimura ◽  
Hiroshi Tsubouchi ◽  
Yasuo Nagaoka ◽  
Kiyoshi Tomioka
Keyword(s):  
Total Synthesis ◽  
Cyclization Reaction ◽  
Neplanocin A ◽  
Tandem Cyclization

Synthesis of Carbocyclic Nucleosides (+)-Neplanocin A, (+)-Aristeromycin and 4'-epi-(+)-Aristeromycin from D-Fructose

2019 ◽  
Vol 16 (9) ◽  
pp. 750-758
Author(s):  
Perali R. Sridhar ◽  
Vennam D.K. Reddy ◽  
Mandava Suresh ◽  
Nadiveedhi M. Reddy ◽  
K. Shiva Kumar
Keyword(s):  
Total Synthesis ◽  
Allylic Alcohol ◽  
Starting Material ◽  
Carbocyclic Nucleosides ◽  
Ring Closing Metathesis ◽  
Neplanocin A ◽  
Oxidative Rearrangement ◽  
Key Steps

D-Fructose is used as the chiral pool starting material for the stereoselective total synthesis of (+)-neplanocin A. Zinc mediated fragmentation, ring-closing metathesis and oxidative rearrangement of cyclic tertiary allylic alcohol are used as the key steps in achieving the synthesis of key carbocylic intermediate. Further, stereoselective total synthesis of 4'-epi-(+)-aristeromycin and the conversion of (+)-neplanocin A to a mixture of (+)-aristeromycin and 4'-epi-(+)-aristeromycin are described.

Total synthesis of (−)-neplanocin A

1983 ◽  
Vol 24 (50) ◽  
pp. 5559-5562 ◽  
Author(s):  
Mu-Ill Lim ◽  
Victor E Marquez
Keyword(s):  
Total Synthesis ◽  
Neplanocin A

ChemInform Abstract: Total Synthesis of (-)-Neplanocin A (I).

ChemInform ◽  
1989 ◽  
Vol 20 (20) ◽  
Author(s):  
V. E. MARQUEZ ◽  
M.-I. LIM ◽  
C. K.-H. TSENG ◽  
A. MARKOVAC ◽  
M. A. PRIEST ◽  
...  
Keyword(s):  
Total Synthesis ◽  
Neplanocin A

ChemInform Abstract: Total Synthesis of (-)-Neplanocin A (I) from L-Ribulose.

ChemInform ◽  
2010 ◽  
Vol 23 (26) ◽  
pp. no-no
Author(s):  
K. VANHESSCHE ◽  
C. G. BELLO ◽  
M. VANDEWALLE
Keyword(s):  
Total Synthesis ◽  
Neplanocin A
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