REGISTRATION

I'm a paragraph. Click here to add your own text and edit me. It’s easy. Just click “Edit Text” or double click me to add your own content and make changes to the font. I’m a great place for you to tell a story and let your users know a little more about you.

UNAFFILIATED
$20

 

I'm a paragraph. Click here to add your own text and edit me. It’s easy. Just click “Edit Text” or double click me to add your own content and make changes to the font. I’m a great place for you to tell a story and let your users know a little more about you.

ACADEMIC
$20

 

I'm a paragraph. Click here to add your own text and edit me. It’s easy. Just click “Edit Text” or double click me to add your own content and make changes to the font. I’m a great place for you to tell a story and let your users know a little more about you.

INDUSTRY
$80

 

I'm a paragraph. Click here to add your own text and edit me. It’s easy. Just click “Edit Text” or double click me to add your own content and make changes to the font. I’m a great place for you to tell a story and let your users know a little more about you.

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Enantioselective Total Synthesis of (+)-Psiguadial B

Enantioselective Total Synthesis of (+)-Psiguadial B

The first enantioselective total synthesis of the cytotoxic natural product (+)-psiguadial B is reported. Key features of the synthesis include (1) the enantioselective preparation of a key cyclobutane intermediate by a tandem Wolff rearrangement/asymmetric ketene addition, (2) a directed C(sp3)–H alkenylation reaction to strategically forge the C1–C2 bond, and (3) a ring-closing metathesis to build the bridging bicyclo[4.3.1]decane terpene framework.

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title

Add a Title