DR ANTHONY MELVIN CRASTO,WorldDrugTracker, helping millions, A 90 % paralysed man in action for you, I am suffering from transverse mylitis and bound to a wheel chair, With death on the horizon, nothing will not stop me except God................DR ANTHONY MELVIN CRASTO Ph.D ( ICT, Mumbai) , INDIA 25Yrs Exp. in the feld of Organic Chemistry,Working for GLENMARK GENERICS at Navi Mumbai, INDIA. Serving chemists around the world. Helping them with websites on Chemistry.Million hits on google, world acclamation from industry, academia, drug authorities for websites, blogs and educational contribution
Showing posts with label bicyclo[1.1.1]pentan-1 -amine. Show all posts
Showing posts with label bicyclo[1.1.1]pentan-1 -amine. Show all posts

Friday, 15 January 2016

Bicyclo[1.1.1]pentan-1 -amine




Bicyclo[1.1.1]pentan-1-amine
177287-49-9 [RN]
22287-35-0 [RN]
Bicyclo[1.1.1]pentan-1-amine hydrochloride
Org Lett. 2014 Apr 4;16(7):1884-7. doi: 10.1021/ol500635p. Epub 2014 Mar 14.

A new route to bicyclo[1.1.1]pentan-1-amine from 1-azido-3-iodobicyclo[1.1.1]pentane.

 http://pubs.acs.org/doi/abs/10.1021/ol500635p

Abstract

From a medicinal chemistry perspective, bicyclo[1.1.1]pentan-1-amine (1) has served as a unique and important moiety. Synthetically, however, this compound has received little attention, and only one scalable route to this amine has been demonstrated. Reduction of an easily available and potentially versatile intermediate, 1-azido-3-iodobicyclo[1.1.1]pentane (2), can offer both a flexible and scalable alternative to this target. Herein, we describe our scrutiny of this reportedly elusive transformation and report our ensuing success with this endeavor.







Abstract Image - See more at: http://organicsynthesisinternational.blogspot.in/#sthash.ZJXPNU5S.dpuf
Org Lett. 2014 Apr 4;16(7):1884-7. doi: 10.1021/ol500635p. Epub 2014 Mar 14.

A new route to bicyclo[1.1.1]pentan-1-amine from 1-azido-3-iodobicyclo[1.1.1]pentane.

 http://pubs.acs.org/doi/abs/10.1021/ol500635p

Abstract

From a medicinal chemistry perspective, bicyclo[1.1.1]pentan-1-amine (1) has served as a unique and important moiety. Synthetically, however, this compound has received little attention, and only one scalable route to this amine has been demonstrated. Reduction of an easily available and potentially versatile intermediate, 1-azido-3-iodobicyclo[1.1.1]pentane (2), can offer both a flexible and scalable alternative to this target. Herein, we describe our scrutiny of this reportedly elusive transformation and report our ensuing success with this endeavor.







Abstract Image - See more at: http://organicsynthesisinternational.blogspot.in/#sthash.ZJXPNU5S.dpuf
Org Lett. 2014 Apr 4;16(7):1884-7. doi: 10.1021/ol500635p. Epub 2014 Mar 14.

A new route to bicyclo[1.1.1]pentan-1-amine from 1-azido-3-iodobicyclo[1.1.1]pentane.

 http://pubs.acs.org/doi/abs/10.1021/ol500635p

 http://pubs.acs.org/doi/suppl/10.1021/ol500635p/suppl_file/ol500635p_si_001.pdf

Abstract

From a medicinal chemistry perspective, bicyclo[1.1.1]pentan-1-amine (1) has served as a unique and important moiety. Synthetically, however, this compound has received little attention, and only one scalable route to this amine has been demonstrated. Reduction of an easily available and potentially versatile intermediate, 1-azido-3-iodobicyclo[1.1.1]pentane (2), can offer both a flexible and scalable alternative to this target. Herein, we describe our scrutiny of this reportedly elusive transformation and report our ensuing success with this endeavor.






Abstract Image

Org Lett. 2014 Apr 4;16(7):1884-7. doi: 10.1021/ol500635p. Epub 2014 Mar 14.

A new route to bicyclo[1.1.1]pentan-1-amine from 1-azido-3-iodobicyclo[1.1.1]pentane.

 http://pubs.acs.org/doi/abs/10.1021/ol500635p

Abstract

From a medicinal chemistry perspective, bicyclo[1.1.1]pentan-1-amine (1) has served as a unique and important moiety. Synthetically, however, this compound has received little attention, and only one scalable route to this amine has been demonstrated. Reduction of an easily available and potentially versatile intermediate, 1-azido-3-iodobicyclo[1.1.1]pentane (2), can offer both a flexible and scalable alternative to this target. Herein, we describe our scrutiny of this reportedly elusive transformation and report our ensuing success with this endeavor.







Abstract Image - See more at: http://organicsynthesisinternational.blogspot.in/#sthash.ZJXPNU5S.dpuf































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 SRILANKAN FOOD


What Is Sri Lankan Food Anyway?

20130304-san-rasa-hoppers.jpg
Hoppers at San Rasa.
Sri Lanka is a small island off the Indian subcontinent, and its cuisine bears similarities to those of both northern and southern India. Describing Sri Lankan food in full demands an article of its own, but here's a brief take on what you can expect to find on Staten Island.
Saucy curries are staples, often enriched with coconut milk and a spice mixture that might veer towards spicy, pungent, or sweet. The curries (meat, fish, and vegetarian) come with rice and vegetable sides like bitter melon and string beans.
Some dishes are composed of starchy mains with strong sauces and relishes on the side. The most famous of these are hoppers, fermented rice flour batter cooked in dome-shaped molds, then stacked up with an egg set in one. String hoppers are nests of rice flour noodles that are steamed and often sold in large quantities; pithu is a log of rice steamed with shredded coconut—the good ones are nutty-sweet and a little bouncy. All of these items can be eaten by hand, with sauces used for dipping.
There are also snacks sometimes called "short eats": fried lentil cakes similar to spiced Indian vadai (savory doughnuts), several types of roti, and fried vegetable and fish cutlets. A more substantial item, and one of my favorites: kotthu, chopped up starch—string hoppers or roti typically—stir fried with aromatic vegetables, egg, spices, and sometimes meat. Stir fried meats are sometimes called devilled, meaning they come in a sweet and spicy sauce not unlike some Chinese dishes.
20130304-san-rasa.jpg
Lamprie at San Rasa.



 

 
 

 

 

 


 

 


 

 

 
 

 
 
 
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